Canonical Allele Identifier: PA2741978393
Gene: ABCG8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2565407
ClinVar RCV Id: RCV003301862
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071882.1:p.Tyr567Ser
CA46471394
NM_022437.3:c.1700A>C