Canonical Allele Identifier: PA913196569
Gene: ABCB11 HGNC NCBI

Linked Data

ClinVar Variation Id: 597818
ClinVar RCV Id: RCV000734053

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003733.2:p.Trp846Cys
CA349126400
NM_003742.4:c.2538G>T
CA349126412
NM_003742.4:c.2538G>C