Allele Registry

Canonical Allele Identifier: PA2579930623

Gene: HRAS HGNC NCBI

ClinVar RCV:

RCV000443979

RCV002060067

ClinVar Variation:

391700

HGVS (amino-acid)	Matching Registered Transcripts
NP_001123914.1:p.Gly60Val	CA16606948 NM_001130442.3:c.179G>T