Canonical Allele Identifier: PA1139693324
Gene: SLC26A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 910782
ClinVar RCV Id: RCV001162817 RCV001162818 RCV001836967
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000432.1:p.Gly707Arg
CA164228038
NM_000441.2:c.2119G>A
CA368845570
NM_000441.2:c.2119G>C