Canonical Allele Identifier: PA2580115105
Gene: SLC26A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1698554
ClinVar RCV Id: RCV002271831
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000432.1:p.Ala434Thr
CA4432772
NM_000441.2:c.1300G>A