Allele Registry

Canonical Allele Identifier: PA295248

Gene: HRAS HGNC NCBI

Linked Data - Variant Effect Evidence

MaveDb:

Score 0.0772290436

Score 0.0958354844

Score -0.0788204442

Score 0.4831430509

Linked Data - NCBI & NCI

ClinVar Allele:

27645

ClinVar RCV:

RCV000013440

RCV000149831

RCV000207504

RCV000417661

RCV000420958

RCV000423190

RCV000424247

RCV000425964

RCV000426653

RCV000428812

RCV000431688

RCV000433893

RCV000434069

RCV000436007

RCV000436205

RCV000439052

RCV000439954

RCV000441514

RCV000444110

RCV000445225

RCV000445336

RCV000678903

RCV000762847

RCV001813188

RCV003421918

ClinVar Variation:

12606

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_005334.1:p.Gly13Cys	CA295247 NM_005343.4:c.37G>T