Canonical Allele Identifier: PA2741817524
Gene: SLC26A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2663014
ClinVar RCV Id: RCV003441679
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000432.1:p.Gly334Trp
CA4432641
NM_000441.2:c.1000G>T