Canonical Allele Identifier: PA2580114883
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 1758541
ClinVar RCV Id: RCV002380337

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Leu2457Met
CA345997304
NM_000384.3:c.7369C>A