Canonical Allele Identifier: PA645387606
Gene: SLC26A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 402277
ClinVar RCV Id: RCV000454307 RCV002522746 RCV001004649
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000432.1:p.Phe683Ser
CA16609565
NM_000441.2:c.2048T>C