Canonical Allele Identifier: PA2580115025
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 1768460

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Arg3291Cys
CA066925
NM_000384.3:c.9871C>T