Allele Registry

Canonical Allele Identifier: PA2580198907

Gene: HRAS HGNC NCBI

ClinVar RCV:

RCV002885723

RCV003395528

ClinVar Variation:

2037387

HGVS (amino-acid)	Matching Registered Transcripts
NP_001304983.1:p.Gly43Ser	CA378922726 NM_001318054.2:c.127G>A