Canonical Allele Identifier: PA2827259051
Gene: ADAMTS18 HGNC NCBI
ClinVar RCV:
RCV001209368
ClinVar Variation:
939891
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001313287.1:p.Tyr1037Asp
CA396829389
NM_001326358.2:c.3109T>G