Canonical Allele Identifier: PA645387700
Gene: SLC26A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 228396

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000432.1:p.Asp724Gly
CA4433064
NM_000441.2:c.2171A>G