Canonical Allele Identifier: PA2828052919
Gene: ABCG8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2628634
ClinVar RCV Id: RCV003399590
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001344250.1:p.Ala549Val
CA1637578
NM_001357321.2:c.1646C>T