Canonical Allele Identifier: PA2826646738
Gene: ADAM33 HGNC NCBI

Linked Data

ClinVar Variation Id: 2536309
ClinVar RCV Id: RCV004308868
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269376.1:p.Ser786Cys
CA9745033
NM_001282447.3:c.2356A>T