Canonical Allele Identifier: PA645387508
Gene: SLC26A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 229254
ClinVar RCV Id: RCV001828084 RCV002478773 RCV003230455 RCV000215204
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000432.1:p.Asp560Asn
CA4432908
NM_000441.2:c.1678G>A