Canonical Allele Identifier: PA2573167872
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 1493094
ClinVar RCV Id: RCV001984110
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Ser4244Pro
CA345970605
NM_000384.3:c.12730T>C