Canonical Allele Identifier: PA2573170093
Gene: SLC26A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1685126
ClinVar RCV Id: RCV002248218 RCV002488628 RCV003560883
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000432.1:p.Tyr375Cys
CA4432685
NM_000441.2:c.1124A>G