Canonical Allele Identifier: PA2580115205
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 1770071
ClinVar RCV Id: RCV002385854

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Asn4431Lys
CA345967797
NM_000384.3:c.13293C>G
CA345967800
NM_000384.3:c.13293C>A