Canonical Allele Identifier: PA2580115192
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 2495927
ClinVar RCV Id: RCV004285219
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Leu4302Pro
CA345970234
NM_000384.3:c.12905T>C