Canonical Allele Identifier: PA1139693336
Gene: SLC26A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 949741
ClinVar RCV Id: RCV001221275 RCV001375680 RCV003331083
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000432.1:p.His723Asp
CA368845871
NM_000441.2:c.2167C>G