Allele Registry

Canonical Allele Identifier: PA916071670

Gene: HRAS HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000013431

RCV000013432

RCV000013433

RCV000032850

RCV000157912

RCV000322736

RCV000428111

RCV000438340

RCV001577794

RCV001732216

RCV003415692

RCV004018622

ClinVar Variation:

12600

279921

1209208

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_789765.1:p.Gly12Val	CA122545 NM_176795.5:c.35G>T CA10603217 NM_176795.5:c.35_36delinsTA CA658795203 NM_176795.5:c.35_36delinsTT CA2695212980 NM_176795.5:c.35_36delinsTG