Allele Registry

Canonical Allele Identifier: PA2579933352

Gene: HRAS HGNC NCBI

ClinVar Allele:

1709539

ClinVar RCV:

RCV002292422

ClinVar Variation:

1711128

HGVS (amino-acid)	Matching Registered Transcripts
NP_001123914.1:p.Asp57Ala	CA378924693 NM_001130442.3:c.170A>C