Allele Registry

Canonical Allele Identifier: PA296058

Gene: HRAS HGNC NCBI

MaveDb:

Score -0.2793198194

Score -0.4231621846

Score -0.1319090997

Score -0.1284484094

ClinVar Allele:

48906

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