Allele Registry

Canonical Allele Identifier: PA2499249451

Gene: MET HGNC NCBI

ClinVar RCV:

RCV001342920

ClinVar Variation:

1039445

HGVS (amino-acid)	Matching Registered Transcripts
NP_001311331.1:p.Thr743Ser	CA368990382 NM_001324402.2:c.2227A>T CA368990385 NM_001324402.2:c.2228C>G