Canonical Allele Identifier: PA2741817196
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 2629900
ClinVar RCV Id: RCV004529814
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Ala1939Thr
CA346003920
NM_000384.3:c.5815G>A