Allele Registry

Canonical Allele Identifier: PA2579932003

Gene: HRAS HGNC NCBI

ClinVar RCV:

RCV000121201

RCV000813562

ClinVar Variation:

134514

HGVS (amino-acid)	Matching Registered Transcripts
NP_001123914.1:p.Thr158Met	CA160026 NM_001130442.3:c.473C>T