Allele Registry

Canonical Allele Identifier: PA2829601154

Gene: HRAS HGNC NCBI

ClinVar RCV:

RCV001203653

RCV001813581

ClinVar Variation:

935131

HGVS (amino-acid)	Matching Registered Transcripts
NP_005334.1:p.Leu168Pro	CA5779216 NM_005343.4:c.503T>C