Canonical Allele Identifier: PA2580115148
Gene: SLC26A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2185667
ClinVar RCV Id: RCV002632554

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000432.1:p.Asn579Ser
CA368842874
NM_000441.2:c.1736A>G