Canonical Allele Identifier: PA915966719
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 653209
ClinVar RCV Id: RCV000808940

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120972.1:p.Ser773Gly
CA368981891
NM_001127500.3:c.2317A>G