Allele Registry

Canonical Allele Identifier: PA2579932771

Gene: HRAS HGNC NCBI

ClinVar RCV:

RCV002027674

ClinVar Variation:

1520643

HGVS (amino-acid)	Matching Registered Transcripts
NP_001123914.1:p.Arg123His	CA378923299 NM_001130442.3:c.368G>A