Canonical Allele Identifier: PA2825617656
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_001120972.1:p.Thr17Ser
CA164887693
NM_001127500.3:c.50C>G
CA368968231
NM_001127500.3:c.49A>T