Canonical Allele Identifier: PA2499232511
Gene: SLC26A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1187576

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000432.1:p.Leu743Ser
CA368846153
NM_000441.2:c.2228T>C