Canonical Allele Identifier: PA109730
Gene: SLC26A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 4835
ClinVar RCV Id: RCV000005106 RCV000036493 RCV000413949 RCV000824762 RCV001375189 RCV001813952 RCV004528079
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000432.1:p.Val138Phe
CA253312
NM_000441.2:c.412G>T