Canonical Allele Identifier: PA093766
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 13890
ClinVar RCV Id: RCV000014904
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000236.2:p.Lys1244Arg
CA123614
NM_000245.4:c.3731A>G