Canonical Allele Identifier: PA658809102
Gene: ABCG8 HGNC NCBI

Linked Data

ClinVar Variation Id: 499929
ClinVar RCV Id: RCV000596406 RCV001137121 RCV003330815 RCV003952976
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071882.1:p.Met429Val
CA1637390
NM_022437.3:c.1285A>G