Canonical Allele Identifier: PA2580114600
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 1730758
ClinVar RCV Id: RCV002451767 RCV003099436
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Ser1125Ala
CA058680
NM_000384.3:c.3373T>G