Canonical Allele Identifier: PA915964248
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 255990

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Ser3294Pro
CA066933
NM_000384.3:c.9880T>C