Canonical Allele Identifier: PA2825621254
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 2008516
ClinVar RCV Id: RCV002828675

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120972.1:p.Thr1010Ser
CA368987276
NM_001127500.3:c.3028A>T
CA368987278
NM_001127500.3:c.3029C>G