Canonical Allele Identifier: PA109653
Gene: SLC26A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 4826
ClinVar RCV Id: RCV000005097 RCV000005096 RCV000154350 RCV001057908
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000432.1:p.Thr721Met
CA253308
NM_000441.2:c.2162C>T