Allele Registry

Canonical Allele Identifier: PA2573200961

Gene: MET HGNC NCBI

ClinVar RCV:

RCV001913968

RCV004044041

ClinVar Variation:

1420031

HGVS (amino-acid)	Matching Registered Transcripts
NP_001311331.1:p.Lys814Thr	CA368991796 NM_001324402.2:c.2441A>C