Allele Registry

Canonical Allele Identifier: PA2579932411

Gene: HRAS HGNC NCBI

ClinVar RCV:

RCV001953316

ClinVar Variation:

1443090

HGVS (amino-acid)	Matching Registered Transcripts
NP_001123914.1:p.Arg123Gly	CA378923304 NM_001130442.3:c.367C>G