Canonical Allele Identifier: PA658803110
Gene: SLC26A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 504923
ClinVar RCV Id: RCV000611863 RCV000664751 RCV001785682 RCV002506451 RCV002529307
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000432.1:p.Arg43His
CA4432368
NM_000441.2:c.128G>A