Allele Registry

Canonical Allele Identifier: PA2830359767

Gene: HRAS HGNC NCBI

ClinVar RCV:

RCV001953316

ClinVar Variation:

1443090

HGVS (amino-acid)	Matching Registered Transcripts
NP_789765.1:p.Arg123Gly	CA378923304 NM_176795.5:c.367C>G