Canonical Allele Identifier: PA2825148592
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 3231440
ClinVar RCV Id: RCV004525511
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Gln2173Glu
CA063313
NM_000384.3:c.6517C>G