Canonical Allele Identifier: PA2573170057
Gene: SLC26A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1513051
ClinVar RCV Id: RCV002045808
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000432.1:p.Ser252Phe
CA4432557
NM_000441.2:c.755C>T