Canonical Allele Identifier: PA093836
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 13885
ClinVar RCV Id: RCV000014899 RCV000441479 RCV000430628 RCV000420374 RCV001851861 RCV002362584
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000236.2:p.Tyr1230Cys
CA257003
NM_000245.4:c.3689A>G