Canonical Allele Identifier: PA2825103601
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 1509000
ClinVar RCV Id: RCV002016520
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000236.2:p.Lys957Met
CA368986748
NM_000245.4:c.2870A>T