Canonical Allele Identifier: PA132704
Gene: SLC26A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 43539
ClinVar RCV Id: RCV000036474 RCV000668787 RCV001785462
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000432.1:p.Asp711Asn
CA132703
NM_000441.2:c.2131G>A