Canonical Allele Identifier: PA916062658
Gene: ADAMTS18 HGNC NCBI

Linked Data

ClinVar Variation Id: 770636
ClinVar RCV Id: RCV000949816
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_955387.1:p.Ala594Thr
CA8181163
NM_199355.4:c.1780G>A