Allele Registry

Canonical Allele Identifier: PA2579931177

Gene: HRAS HGNC NCBI

ClinVar RCV:

RCV001232757

RCV004033178

ClinVar Variation:

959406

HGVS (amino-acid)	Matching Registered Transcripts
NP_001123914.1:p.Pro140Leu	CA378922896 NM_001130442.3:c.419C>T