Canonical Allele Identifier: PA2580114804
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 1751050
ClinVar RCV Id: RCV002358037

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Asp2003Tyr
CA346003500
NM_000384.3:c.6007G>T