Allele Registry

Canonical Allele Identifier: PA916071652

Gene: HRAS HGNC NCBI

ClinVar RCV:

RCV000150836

RCV000255809

ClinVar Variation:

163690

HGVS (amino-acid)	Matching Registered Transcripts
NP_789765.1:p.Gly12Glu	CA273158 NM_176795.5:c.35_36delinsAA