Allele Registry

Canonical Allele Identifier: PA2580198906

Gene: HRAS HGNC NCBI

ClinVar RCV:

RCV003089864

ClinVar Variation:

2162148

HGVS (amino-acid)	Matching Registered Transcripts
NP_001304983.1:p.Pro40Leu	CA472429329 NM_001318054.2:c.119C>T