Canonical Allele Identifier: PA110991
Gene: ABCG8 HGNC NCBI

Linked Data

ClinVar Variation Id: 4970
ClinVar RCV Id: RCV000005258 RCV000727975 RCV003407279
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071882.1:p.Arg263Gln
CA253364
NM_022437.3:c.788G>A