Canonical Allele Identifier: PA180611
Gene: SLC26A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 177682
ClinVar RCV Id: RCV000154281
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000432.1:p.Lys531Thr
CA180610
NM_000441.2:c.1592A>C