Canonical Allele Identifier: PA2825102681
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 216499
ClinVar RCV Id: RCV000200572 RCV001011655 RCV001293439 RCV003148673 RCV003320597 RCV003468909
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000236.2:p.His484Arg
CA339400
NM_000245.4:c.1451A>G