Canonical Allele Identifier: PA645387502
Gene: SLC26A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 370114
ClinVar RCV Id: RCV000410361 RCV001386694 RCV003475938
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000432.1:p.Ser532Ile
CA16041114
NM_000441.2:c.1595G>T