Allele Registry

Canonical Allele Identifier: PA2825104017

Gene: MET HGNC NCBI

ClinVar RCV:

RCV001342920

ClinVar Variation:

1039445

HGVS (amino-acid)	Matching Registered Transcripts
NP_000236.2:p.Thr1173Ser	CA368990382 NM_000245.4:c.3517A>T CA368990385 NM_000245.4:c.3518C>G