Canonical Allele Identifier: PA645440709
Gene: ABCG8 HGNC NCBI

Linked Data

ClinVar Variation Id: 336063
ClinVar RCV Id: RCV000403947 RCV000967641 RCV002374580 RCV003922455
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071882.1:p.Ser32Gly
CA1636886
NM_022437.3:c.94A>G