Canonical Allele Identifier: PA109217
Gene: SLC26A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 43496
ClinVar RCV Id: RCV000036428 RCV000169222 RCV000424441 RCV000515653 RCV000506765 RCV001291345 RCV001814024 RCV002496559
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000432.1:p.Arg409His
CA261401
NM_000441.2:c.1226G>A