Canonical Allele Identifier: PA2826646722
Gene: ADAM33 HGNC NCBI

Linked Data

ClinVar Variation Id: 2275513
ClinVar RCV Id: RCV004130650
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269376.1:p.His562Asp
CA9745278
NM_001282447.3:c.1684C>G