Allele Registry

Canonical Allele Identifier: PA2826977480

Gene: HRAS HGNC NCBI

ClinVar RCV:

RCV002027674

ClinVar Variation:

1520643

HGVS (amino-acid)	Matching Registered Transcripts
NP_001304983.1:p.Ala17Thr	CA378923299 NM_001318054.2:c.49G>A