Canonical Allele Identifier: PA2580115193
Gene: SLC26A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2287795
ClinVar RCV Id: RCV002832016

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000432.1:p.Gln736Pro
CA368846054
NM_000441.2:c.2207A>C