Canonical Allele Identifier: PA916075768
Gene: SLC26A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 725873
ClinVar RCV Id: RCV000900008 RCV002502648
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_998778.1:p.Arg504His
CA2801364
NM_213613.4:c.1511G>A