Canonical Allele Identifier: PA645428069
Gene: SLC26A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 358553
ClinVar RCV Id: RCV000286342 RCV001861297 RCV002523580
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000102.1:p.His237Gln
CA4434057
NM_000111.3:c.711C>G
CA368853131
NM_000111.3:c.711C>A