Canonical Allele Identifier: PA915963614
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 255979
ClinVar RCV Id: RCV000243074 RCV000337679 RCV000407187 RCV000845575 RCV000985334 RCV001094705 RCV001837799 RCV002401954
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Arg532Trp
CA053978
NM_000384.3:c.1594C>T