Canonical Allele Identifier: PA645387338
Gene: SLC26A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 372827
ClinVar RCV Id: RCV000413685

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000432.1:p.Ala362Asp
CA16042657
NM_000441.2:c.1085C>A