Allele Registry

Canonical Allele Identifier: PA2825104123

Gene: MET HGNC NCBI

ClinVar RCV:

RCV001913968

RCV004044041

ClinVar Variation:

1420031

HGVS (amino-acid)	Matching Registered Transcripts
NP_000236.2:p.Lys1244Thr	CA368991796 NM_000245.4:c.3731A>C