Canonical Allele Identifier: PA658803141
Gene: SLC26A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 501589
ClinVar RCV Id: RCV000595913

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000432.1:p.Leu743Val
CA4433081
NM_000441.2:c.2227T>G