Canonical Allele Identifier: PA1139677063
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 927954
ClinVar RCV Id: RCV002560118
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Leu2020Arg
CA062809
NM_000384.3:c.6059T>G