Allele Registry

Canonical Allele Identifier: PA2830359822

Gene: HRAS HGNC NCBI

ClinVar RCV:

RCV003105215

ClinVar Variation:

2416003

HGVS (amino-acid)	Matching Registered Transcripts
NP_789765.1:p.Ile142Phe	CA378922871 NM_176795.5:c.424A>T