Canonical Allele Identifier: PA2741817537
Gene: SLC26A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2809546
ClinVar RCV Id: RCV003679999
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000432.1:p.Gln413Leu
CA368839288
NM_000441.2:c.1238A>T