Canonical Allele Identifier: PA915966132
Gene: SLC26A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 691518
ClinVar RCV Id: RCV001004650

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000432.1:p.Leu703Pro
CA368845501
NM_000441.2:c.2108T>C