Allele Registry

Canonical Allele Identifier: PA2825622084

Gene: MET HGNC NCBI

ClinVar RCV:

RCV001342920

ClinVar Variation:

1039445

HGVS (amino-acid)	Matching Registered Transcripts
NP_001120972.1:p.Thr1191Ser	CA368990382 NM_001127500.3:c.3571A>T CA368990385 NM_001127500.3:c.3572C>G