Canonical Allele Identifier: PA645387666
Gene: SLC26A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 358503
ClinVar RCV Id: RCV000391133 RCV000343520 RCV003168553
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000432.1:p.Asn712Ser
CA4433054
NM_000441.2:c.2135A>G