Canonical Allele Identifier: PA2580115212
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 1714145
ClinVar RCV Id: RCV002297128
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Asn4527Ile
CA053283
NM_000384.3:c.13580A>T