Allele Registry

Canonical Allele Identifier: PA3057509678

Gene: HRAS HGNC NCBI

ClinVar RCV:

RCV005107278

ClinVar Variation:

3637849

HGVS (amino-acid)	Matching Registered Transcripts
NP_789765.1:p.Arg149Leu	CA378922732 NM_176795.5:c.446G>T