Canonical Allele Identifier: PA2580114893
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 1759113
ClinVar RCV Id: RCV002391519
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Trp2495Ser
CA345997056
NM_000384.3:c.7484G>C