Canonical Allele Identifier: PA110437
Gene: SLC26A8 HGNC NCBI

Linked Data

ClinVar Variation Id: 50911
ClinVar RCV Id: RCV000043626
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001180405.1:p.Arg954Cys
CA143851
NM_001193476.2:c.2860C>T