Allele Registry

Canonical Allele Identifier: PA2825103183

Gene: MET HGNC NCBI

ClinVar RCV:

RCV002041269

ClinVar Variation:

1518101

HGVS (amino-acid)	Matching Registered Transcripts
NP_000236.2:p.Glu740Asp	CA368980769 NM_000245.4:c.2220A>C CA368980771 NM_000245.4:c.2220A>T