Canonical Allele Identifier: PA2825621236
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 1802753
ClinVar RCV Id: RCV002466028
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120972.1:p.Arg1005Gly
CA368987211
NM_001127500.3:c.3013C>G