Allele Registry

Canonical Allele Identifier: PA916071774

Gene: HRAS HGNC NCBI

ClinVar RCV:

RCV000013434

RCV000022795

RCV000439343

RCV000587258

RCV000681435

RCV001255683

ClinVar Variation:

12601

HGVS (amino-acid)	Matching Registered Transcripts
NP_789765.1:p.Gln61Lys	CA122547 NM_176795.5:c.181C>A