Allele Registry

Canonical Allele Identifier: PA103547

Gene: HRAS HGNC NCBI

ClinVar RCV:

RCV000013443

RCV000143898

RCV000157915

ClinVar Variation:

12609

HGVS (amino-acid)	Matching Registered Transcripts
NP_001123914.1:p.Gln22Lys	CA122553 NM_001130442.3:c.64C>A