Allele Registry

Canonical Allele Identifier: PA2829601052

Gene: HRAS HGNC NCBI

ClinVar RCV:

RCV001232757

RCV004033178

ClinVar Variation:

959406

HGVS (amino-acid)	Matching Registered Transcripts
NP_005334.1:p.Pro140Leu	CA378922896 NM_005343.4:c.419C>T