Canonical Allele Identifier: PA2573062741
Gene: SLC26A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1185668
ClinVar RCV Id: RCV001823277
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000432.1:p.Tyr27His
CA368844981
NM_000441.2:c.79T>C