Canonical Allele Identifier: PA2580115101
Gene: SLC26A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2136214
ClinVar RCV Id: RCV003037061
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000432.1:p.Lys374Arg
CA4432683
NM_000441.2:c.1121A>G