Canonical Allele Identifier: PA2828052701
Gene: ABCG8 HGNC NCBI

Linked Data

ClinVar Variation Id: 500519

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001344250.1:p.Pro386Leu
CA1637324
NM_001357321.2:c.1157C>T