Canonical Allele Identifier: PA2580115023
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 2340063
ClinVar RCV Id: RCV004182933
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Ala3277Val
CA43496915
NM_000384.3:c.9830C>T