Canonical Allele Identifier: PA2573170213
Gene: SLC26A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1524151
ClinVar RCV Id: RCV002031507
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000432.1:p.Ser735Cys
CA368846045
NM_000441.2:c.2204C>G