Canonical Allele Identifier: PA913197498
Gene: ABCG8 HGNC NCBI

Linked Data

ClinVar Variation Id: 595268
ClinVar RCV Id: RCV000730773
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071882.1:p.Pro12Leu
CA1636855
NM_022437.3:c.35C>T