Canonical Allele Identifier: PA2827253382
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 411912
ClinVar RCV Id: RCV000572470 RCV001293447 RCV001292908 RCV001566122 RCV003470498 RCV003492062
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311330.1:p.Pro773Leu
CA4448450
NM_001324401.3:c.2318C>T