Canonical Allele Identifier: PA2825148333
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 3231432
ClinVar RCV Id: RCV004525503

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Ala1975Ser
CA43506084
NM_000384.3:c.5923G>T