Canonical Allele Identifier: PA109699
Gene: SLC26A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 446456
ClinVar RCV Id: RCV000515668 RCV000670962 RCV001731741 RCV001851413
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000432.1:p.Tyr556Cys
CA4432905
NM_000441.2:c.1667A>G