Canonical Allele Identifier: PA1139674814
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 920679
ClinVar RCV Id: RCV002491520
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Gly1122Val
CA346009235
NM_000384.3:c.3365G>T