Allele Registry

Canonical Allele Identifier: PA2499301282

Gene: HRAS HGNC NCBI

ClinVar RCV:

RCV001321198

ClinVar Variation:

1021434

HGVS (amino-acid)	Matching Registered Transcripts
NP_789765.1:p.Arg68Leu	CA378924629 NM_176795.5:c.203G>T