Allele Registry

Canonical Allele Identifier: PA658807657

Gene: HRAS HGNC NCBI

ClinVar RCV:

RCV000598510

RCV001322927

RCV002483665

ClinVar Variation:

503537

HGVS (amino-acid)	Matching Registered Transcripts
NP_005334.1:p.Tyr4Cys	CA5779438 NM_005343.4:c.11A>G