Canonical Allele Identifier: PA2826646721
Gene: ADAM33 HGNC NCBI

Linked Data

ClinVar Variation Id: 2388121
ClinVar RCV Id: RCV004218235
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269376.1:p.Ser559Arg
CA408105321
NM_001282447.3:c.1677C>G
CA408105322
NM_001282447.3:c.1677C>A
CA408105327
NM_001282447.3:c.1675A>C