Canonical Allele Identifier: PA1139758087
Gene: ADAMTS18 HGNC NCBI
ClinVar RCV:
RCV001209368
ClinVar Variation:
939891
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_955387.1:p.Tyr1209Asp
CA396829389
NM_199355.4:c.3625T>G