Canonical Allele Identifier: PA132706
Gene: SLC26A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 43540
ClinVar RCV Id: RCV000036475 RCV000671686 RCV000947056 RCV004534765
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000432.1:p.Ile713Met
CA132705
NM_000441.2:c.2139T>G