Allele Registry

Canonical Allele Identifier: PA916071731

Gene: HRAS HGNC NCBI

ClinVar RCV:

RCV000022798

ClinVar Variation:

29912

HGVS (amino-acid)	Matching Registered Transcripts
NP_789765.1:p.Glu37dup	CA259683 NM_176795.5:c.108_110dup