Canonical Allele Identifier: PA2828052920
Gene: ABCG8 HGNC NCBI

Linked Data

ClinVar Variation Id: 501367

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001344250.1:p.Ala549Thr
CA1637577
NM_001357321.2:c.1645G>A