Allele Registry

Canonical Allele Identifier: PA2825103678

Gene: MET HGNC NCBI

ClinVar RCV:

RCV001878703

ClinVar Variation:

1370848

HGVS (amino-acid)	Matching Registered Transcripts
NP_000236.2:p.Pro1013Arg	CA368987773 NM_000245.4:c.3038C>G