Allele Registry

Canonical Allele Identifier: PA2579932684

Gene: HRAS HGNC NCBI

ClinVar Allele:

2064605

ClinVar RCV:

RCV002846474

ClinVar Variation:

2015677

HGVS (amino-acid)	Matching Registered Transcripts
NP_001123914.1:p.Lys88Glu	CA378924414 NM_001130442.3:c.262A>G