Canonical Allele Identifier: PA916027384
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 485767
ClinVar RCV Id: RCV000567437 RCV000821666 RCV001293997
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311330.1:p.Ser548Leu
CA4448215
NM_001324401.3:c.1643C>T