Canonical Allele Identifier: PA2741817230
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 2940190
ClinVar RCV Id: RCV003797548

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Leu2231Ser
CA346001004
NM_000384.3:c.6692T>C