Canonical Allele Identifier: PA2580114885
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 2451329
ClinVar RCV Id: RCV003182345

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Leu2459Gln
CA345997291
NM_000384.3:c.7376T>A