Allele Registry

Canonical Allele Identifier: PA2741862003

Gene: MET HGNC NCBI

ClinVar RCV:

RCV003369926

ClinVar Variation:

2612857

HGVS (amino-acid)	Matching Registered Transcripts
NP_001311331.1:p.Val790Phe	CA368991472 NM_001324402.2:c.2368G>T