Canonical Allele Identifier: PA916027150
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 825439
ClinVar RCV Id: RCV001023537 RCV001223443
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311330.1:p.Thr17Ser
CA164887693
NM_001324401.3:c.50C>G
CA368968231
NM_001324401.3:c.49A>T