Canonical Allele Identifier: PA1139704289
Gene: ABCB11 HGNC NCBI

Linked Data

ClinVar Variation Id: 893254
ClinVar RCV Id: RCV001130868

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003733.2:p.Met805Val
CA349127570
NM_003742.4:c.2413A>G