Allele Registry

Canonical Allele Identifier: PA2825101677

Gene: MET HGNC NCBI

ClinVar RCV:

RCV001023537

RCV001223443

ClinVar Variation:

825439

HGVS (amino-acid)	Matching Registered Transcripts
NP_000236.2:p.Thr17Ser	CA164887693 NM_000245.4:c.50C>G CA368968231 NM_000245.4:c.49A>T