Canonical Allele Identifier: PA2825171300
Gene: SLC26A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 3233466
ClinVar RCV Id: RCV004526316
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000432.1:p.Ser415Ile
CA368839301
NM_000441.2:c.1244G>T