Allele Registry

Canonical Allele Identifier: PA2580532814

Gene: HRAS HGNC NCBI

ClinVar Allele:

1709539

ClinVar RCV:

RCV002292422

ClinVar Variation:

1711128

HGVS (amino-acid)	Matching Registered Transcripts
NP_789765.1:p.Asp57Ala	CA378924693 NM_176795.5:c.170A>C