Allele Registry

Canonical Allele Identifier: PA916022174

Gene: HRAS HGNC NCBI

ClinVar RCV:

RCV000434487

RCV000637302

ClinVar Variation:

40445

HGVS (amino-acid)	Matching Registered Transcripts
NP_001304983.1:p.Asp75Asn	CA5779226 NM_001318054.2:c.223G>A