Canonical Allele Identifier: PA645444749
Gene: ABCB11 HGNC NCBI

Linked Data

ClinVar Variation Id: 332032

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003733.2:p.Val567Ile
CA10612844
NM_003742.4:c.1699G>A