Canonical Allele Identifier: PA2580115217
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 2451292
ClinVar RCV Id: RCV003182308
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Asn4549Lys
CA345966796
NM_000384.3:c.13647C>G
CA345966797
NM_000384.3:c.13647C>A