Allele Registry

Canonical Allele Identifier: PA645475332

Gene: HRAS HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000420757

RCV000422470

RCV000423098

RCV000424391

RCV000427302

RCV000431015

RCV000432499

RCV000432733

RCV000435578

RCV000437532

RCV000442518

RCV000444550

RCV000444619

ClinVar Variation:

376444

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_005334.1:p.Gln61Glu	CA16602879 NM_005343.4:c.181C>G