Canonical Allele Identifier: PA2825149503
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 3231483
ClinVar RCV Id: RCV004525554

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Leu3313Pro
CA345988224
NM_000384.3:c.9938T>C