Canonical Allele Identifier: PA274439
Gene: SLC26A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 189160
ClinVar RCV Id: RCV000169586 RCV000515656 RCV003556213
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000432.1:p.Ile529Ser
CA274438
NM_000441.2:c.1586T>G