Canonical Allele Identifier: PA2826592667
Gene: SLC26A6 HGNC NCBI

Linked Data

ClinVar Variation Id: 64457
ClinVar RCV Id: RCV000054644
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268661.1:p.Arg193Pro
CA216183
NM_001281732.2:c.578G>C