Canonical Allele Identifier: PA2825171999
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_000434.1:p.Leu1279_Ter1280insArgThrPheAlaThrValTyrPheLysAsnLysPheLysLeuPheTyrHisPheIle
CA10606615
NM_000443.4:c.3838T>C
CA368056241
NM_000443.4:c.3838T>A