Allele Registry

Canonical Allele Identifier: PA2825102221

Gene: MET HGNC NCBI

ClinVar RCV:

RCV002427840

RCV003103482

ClinVar Variation:

1762344

HGVS (amino-acid)	Matching Registered Transcripts
NP_000236.2:p.Thr273Ile	CA164889071 NM_000245.4:c.818C>T