Canonical Allele Identifier: PA2828052993
Gene: ABCG8 HGNC NCBI

Linked Data

ClinVar Variation Id: 4973
ClinVar RCV Id: RCV000005261

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001344250.1:p.Leu595Arg
CA253368
NM_001357321.2:c.1784T>G