Canonical Allele Identifier: PA132708
Gene: SLC26A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 43543

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000432.1:p.Gln730His
CA132707
NM_000441.2:c.2190G>T
CA368845981
NM_000441.2:c.2190G>C