Allele Registry

Canonical Allele Identifier: PA1139748281

Gene: HRAS HGNC NCBI

ClinVar Allele:

935599

ClinVar RCV:

RCV001204299

ClinVar Variation:

935657

HGVS (amino-acid)	Matching Registered Transcripts
NP_789765.1:p.Lys88Arg	CA378924406 NM_176795.5:c.263A>G