Canonical Allele Identifier: PA1139695729
Gene: ADAMTS18 HGNC NCBI
ClinVar RCV:
RCV001044523
ClinVar Variation:
842151
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001313287.1:p.Pro947Ala
CA8180487
NM_001326358.2:c.2839C>G