Canonical Allele Identifier: PA2825103609
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 1520569
ClinVar RCV Id: RCV002030834
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000236.2:p.Gln960His
CA368986795
NM_000245.4:c.2880A>C
CA368986797
NM_000245.4:c.2880A>T