Canonical Allele Identifier: PA2580114878
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 1758133
ClinVar RCV Id: RCV002382708 RCV003776372
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.His2433Leu
CA064294
NM_000384.3:c.7298A>T