Canonical Allele Identifier: PA915964333
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 440521
ClinVar RCV Id: RCV000508761
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Glu3553Lys
CA044247
NM_000384.3:c.10657G>A