Canonical Allele Identifier: PA645387678
Gene: SLC26A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 381687
ClinVar RCV Id: RCV000441837 RCV000984219 RCV002282143
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000432.1:p.Phe718Ser
CA4433060
NM_000441.2:c.2153T>C