Canonical Allele Identifier: PA256993
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 13881
ClinVar RCV Id: RCV000014895 RCV000565834 RCV002228027
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120972.1:p.Met1149Thr
CA256991
NM_001127500.3:c.3446T>C