Canonical Allele Identifier: PA2829919656
Gene: ABCB4 HGNC NCBI

Linked Data

ClinVar Variation Id: 289975
ClinVar RCV Id: RCV000726408 RCV003485571
ClinVar Variation Id: 3064147
ClinVar RCV Id: RCV003988735
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061337.1:p.Leu1286_Ter1287insArgThrPheAlaThrValTyrPheLysAsnLysPheLysLeuPheTyrHisPheIle
CA10606615
NM_018849.3:c.3859T>C
CA368056241
NM_018849.3:c.3859T>A