Canonical Allele Identifier: PA2741817059
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 2926454
ClinVar RCV Id: RCV003788692
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Gly1122Ser
CA058667
NM_000384.3:c.3364G>A