Canonical Allele Identifier: PA915964043
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 630611

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Arg2444His
CA064309
NM_000384.3:c.7331G>A