Allele Registry

Canonical Allele Identifier: PA2579933177

Gene: HRAS HGNC NCBI

ClinVar RCV:

RCV000207497

ClinVar Variation:

40438

HGVS (amino-acid)	Matching Registered Transcripts
NP_001123914.1:p.Ser89Cys	CA351483 NM_001130442.3:c.266C>G