Canonical Allele Identifier: PA2828509822
Gene: ATP8B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 286355
ClinVar RCV Id: RCV000384110 RCV004547708
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361314.1:p.Thr1242Ser
CA8973924
NM_001374385.1:c.3725C>G
CA402539329
NM_001374385.1:c.3724A>T