Canonical Allele Identifier: PA658826995
Gene: SLC26A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 552468
ClinVar RCV Id: RCV000667731 RCV001226428 RCV003472089
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000432.1:p.Leu729Pro
CA164228145
NM_000441.2:c.2186T>C