Canonical Allele Identifier: PA261422
Gene: SLC26A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 43528
ClinVar RCV Id: RCV000036463 RCV000675129 RCV001731331 RCV003473269 RCV003727609
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000432.1:p.Ile655Val
CA261421
NM_000441.2:c.1963A>G