Canonical Allele Identifier: PA658668660
Gene: SLC26A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 446454
ClinVar RCV Id: RCV000515726 RCV000668348
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000432.1:p.Thr527Pro
CA368841594
NM_000441.2:c.1579A>C