Canonical Allele Identifier: PA2825148865
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 3127916
ClinVar RCV Id: RCV004417749
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Phe2430Tyr
CA345997481
NM_000384.3:c.7289T>A