Canonical Allele Identifier: PA109294
Gene: SLC26A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 43519
ClinVar RCV Id: RCV000036454 RCV000666339 RCV001004646 RCV001781350
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000432.1:p.Cys565Tyr
CA261418
NM_000441.2:c.1694G>A