Canonical Allele Identifier: PA2573167719
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 1416441
ClinVar RCV Id: RCV001921251
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Asp3540Gly
CA345985894
NM_000384.3:c.10619A>G