Allele Registry

Canonical Allele Identifier: PA2825104051

Gene: MET HGNC NCBI

ClinVar RCV:

RCV001360520

ClinVar Variation:

246643

HGVS (amino-acid)	Matching Registered Transcripts
NP_000236.2:p.Leu1195Phe	CA10584670 NM_000245.4:c.3583C>T