Canonical Allele Identifier: PA109481
Gene: SLC26A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 4842

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000432.1:p.Phe335Leu
CA253316
NM_000441.2:c.1003T>C
CA368838312
NM_000441.2:c.1005T>A
CA368838314
NM_000441.2:c.1005T>G