Canonical Allele Identifier: PA2741817060
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 2681891
ClinVar RCV Id: RCV003477183
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Pro1127Ala
CA346009208
NM_000384.3:c.3379C>G