Canonical Allele Identifier: PA2499232497
Gene: SLC26A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1065085

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000432.1:p.Asn382Lys
CA4432693
NM_000441.2:c.1146C>G
CA368838955
NM_000441.2:c.1146C>A