Canonical Allele Identifier: PA2741817254
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 2928805
ClinVar RCV Id: RCV003789579
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Met2422Thr
CA345997536
NM_000384.3:c.7265T>C