Canonical Allele Identifier: PA2580114887
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 1758682
ClinVar RCV Id: RCV002380478
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Leu2466Val
CA345997248
NM_000384.3:c.7396T>G