Canonical Allele Identifier: PA2825148541
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 3231439
ClinVar RCV Id: RCV004525510
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Ala2122Val
CA346001922
NM_000384.3:c.6365C>T