Canonical Allele Identifier: PA2826646723
Gene: ADAM33 HGNC NCBI

Linked Data

ClinVar Variation Id: 3145795
ClinVar RCV Id: RCV004437115
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269376.1:p.Gly581Arg
CA9745259
NM_001282447.3:c.1741G>A
CA408105177
NM_001282447.3:c.1741G>C