Canonical Allele Identifier: PA2580115021
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 1768328
ClinVar RCV Id: RCV002376851
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Pro3275Leu
CA345988631
NM_000384.3:c.9824C>T