Canonical Allele Identifier: PA2580114844
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 1754543
ClinVar RCV Id: RCV002364629
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Leu2209Ser
CA346001304
NM_000384.3:c.6626T>C