Allele Registry

Canonical Allele Identifier: PA296058

Gene: HRAS HGNC NCBI

ClinVar RCV:

RCV000157917

RCV001387769

ClinVar Variation:

40436

HGVS (amino-acid)	Matching Registered Transcripts
NP_005334.1:p.Gly60Asp	CA296057 NM_005343.4:c.179G>A