Canonical Allele Identifier: PA2573318169
Gene: SLC26A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1363882
ClinVar RCV Id: RCV001937220 RCV002490011 RCV004039859
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_998778.1:p.Arg465Gln
CA2801387
NM_213613.4:c.1394G>A