Canonical Allele Identifier: PA2573170210
Gene: SLC26A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1489742
ClinVar RCV Id: RCV002001577

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000432.1:p.Phe718Val
CA368845796
NM_000441.2:c.2152T>G