Allele Registry

Canonical Allele Identifier: PA2825104087

Gene: MET HGNC NCBI

ClinVar RCV:

RCV001553682

ClinVar Variation:

1192249

HGVS (amino-acid)	Matching Registered Transcripts
NP_000236.2:p.Val1220Leu	CA368991469 NM_000245.4:c.3658G>C