Canonical Allele Identifier: PA1139674827
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 928133
ClinVar RCV Id: RCV001859155 RCV002451400
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Leu1148His
CA058872
NM_000384.3:c.3443T>A