Canonical Allele Identifier: PA109417
Gene: SLC26A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 43555
ClinVar RCV Id: RCV000036491 RCV000225040 RCV000225082 RCV000757776 RCV001823104 RCV002504887 RCV004534767
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000432.1:p.Leu117Phe
CA132727
NM_000441.2:c.349C>T