Canonical Allele Identifier: PA1139677965
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 925408
ClinVar RCV Id: RCV003106144
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Glu2414Val
CA064231
NM_000384.3:c.7241A>T