Canonical Allele Identifier: PA109506
Gene: SLC26A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 691506
ClinVar RCV Id: RCV001004620 RCV002469306 RCV003558616
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000432.1:p.Pro123Ser
CA164214883
NM_000441.2:c.367C>T