Canonical Allele Identifier: PA261441
Gene: SLC26A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 43568
ClinVar RCV Id: RCV000036508 RCV000396295 RCV001171537 RCV002477085 RCV003473272
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000432.1:p.Cys282Tyr
CA261440
NM_000441.2:c.845G>A