Canonical Allele Identifier: PA166712
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 141889
ClinVar RCV Id: RCV000130588 RCV001223449 RCV001775623
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120972.1:p.Asp208Gly
CA166710
NM_001127500.3:c.623A>G