Canonical Allele Identifier: PA913200299
Gene: ADAMTS10 HGNC NCBI

Linked Data

ClinVar Variation Id: 595050
ClinVar RCV Id: RCV000730483
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_112219.3:p.Ser1088Gly
CA9159951
NM_030957.3:c.3262A>G