Canonical Allele Identifier: PA2573162879
Gene: SLC26A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1513795
ClinVar RCV Id: RCV002045999
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000103.2:p.Arg279Pro
CA361706395
NM_000112.4:c.836G>C