Canonical Allele Identifier: PA645387639
Gene: SLC26A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 379535
ClinVar RCV Id: RCV000444355
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000432.1:p.Ile700Met
CA16605617
NM_000441.2:c.2100A>G