Canonical Allele Identifier: PA132655
Gene: SLC26A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 43491
ClinVar RCV Id: RCV000036422 RCV000275313 RCV000367654 RCV000906081 RCV004541094
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000432.1:p.Ala357Thr
CA132654
NM_000441.2:c.1069G>A