Canonical Allele Identifier: PA109453
Gene: SLC26A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 4822
ClinVar RCV Id: RCV000005091
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000432.1:p.Lys369Glu
CA253305
NM_000441.2:c.1105A>G