Canonical Allele Identifier: PA261426
Gene: SLC26A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 43541
ClinVar RCV Id: RCV000036476 RCV000585409 RCV000675123 RCV002051802
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000432.1:p.Lys715Asn
CA261425
NM_000441.2:c.2145G>T
CA368845764
NM_000441.2:c.2145G>C