Allele Registry

Canonical Allele Identifier: PA916071819

Gene: HRAS HGNC NCBI

ClinVar RCV:

RCV000494039

RCV000705122

ClinVar Variation:

430506

HGVS (amino-acid)	Matching Registered Transcripts
NP_789765.1:p.Lys101Arg	CA378923959 NM_176795.5:c.302A>G