Canonical Allele Identifier: PA2741817074
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 2931277
ClinVar RCV Id: RCV003782539
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Ala1166Thr
CA346008967
NM_000384.3:c.3496G>A