Canonical Allele Identifier: PA247980
Gene: SLC26A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 199023
ClinVar RCV Id: RCV000180506 RCV001159776 RCV000724401 RCV001159775 RCV003165379
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000432.1:p.Ser347Leu
CA247979
NM_000441.2:c.1040C>T