Canonical Allele Identifier: PA1139679985
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 897107
ClinVar RCV Id: RCV001142061 RCV001140214 RCV001858914
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Pro3281His
CA345988541
NM_000384.3:c.9842C>A