Canonical Allele Identifier: PA102191
Gene: SLC26A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 55975
ClinVar RCV Id: RCV000049384
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000102.1:p.Leu496Arg
CA144059
NM_000111.3:c.1487T>G