Canonical Allele Identifier: PA1139674825
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 922444
ClinVar RCV Id: RCV002339457 RCV002559033
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Ala1144Asp
CA058851
NM_000384.3:c.3431C>A