Canonical Allele Identifier: PA111991
Gene: ABCB11 HGNC NCBI

Linked Data

ClinVar Variation Id: 6595

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003733.2:p.Arg432Thr
CA253880
NM_003742.4:c.1295G>C