Canonical Allele Identifier: PA2580115102
Gene: SLC26A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1804681
ClinVar RCV Id: RCV002469978
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000432.1:p.Ala411Thr
CA368839273
NM_000441.2:c.1231G>A