Allele Registry

Canonical Allele Identifier: PA916022175

Gene: HRAS HGNC NCBI

ClinVar RCV:

RCV000121201

RCV000813562

ClinVar Variation:

134514

HGVS (amino-acid)	Matching Registered Transcripts
NP_001304983.1:p.Thr79Met	CA160026 NM_001318054.2:c.236C>T