Canonical Allele Identifier: PA1139682387
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 920530

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Arg4297Cys
CA051437
NM_000384.3:c.12889C>T