Canonical Allele Identifier: PA144106
Gene: SLC26A3 HGNC NCBI
ClinVar RCV:
RCV000049412
ClinVar Variation:
56003
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000102.1:p.Arg175Ser
CA144104
NM_000111.3:c.525G>C
CA368853510
NM_000111.3:c.525G>T