Canonical Allele Identifier: PA132733
Gene: SLC26A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 43560
ClinVar RCV Id: RCV000036497 RCV000710318 RCV000901389
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000432.1:p.Ala189Ser
CA132732
NM_000441.2:c.565G>T