Canonical Allele Identifier: PA2499249520
Gene: ADAMTS18 HGNC NCBI
ClinVar RCV:
RCV001326386
ClinVar Variation:
1025992
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001313287.1:p.Ser987Asn
CA8180418
NM_001326358.2:c.2960G>A