Canonical Allele Identifier: PA132686
Gene: SLC26A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 43527
ClinVar RCV Id: RCV000036462 RCV000966198 RCV001004781 RCV001159887 RCV004534764
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000432.1:p.Ser642Pro
CA132685
NM_000441.2:c.1924T>C