Canonical Allele Identifier: PA2580114510
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 1791920
ClinVar RCV Id: RCV002430788
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Leu827Pro
CA056527
NM_000384.3:c.2480T>C