Allele Registry

Canonical Allele Identifier: PA2826977521

Gene: HRAS HGNC NCBI

ClinVar RCV:

RCV003627211

ClinVar Variation:

2893865

HGVS (amino-acid)	Matching Registered Transcripts
NP_001304983.1:p.Pro42Ala	CA378922744 NM_001318054.2:c.124C>G