Canonical Allele Identifier: PA132692
Gene: SLC26A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 43531
ClinVar RCV Id: RCV000036466 RCV000671610 RCV001071424 RCV004541096
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000432.1:p.Thr67Ser
CA132691
NM_000441.2:c.200C>G
CA368845363
NM_000441.2:c.199A>T