Canonical Allele Identifier: PA1139674859
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 2930221
ClinVar RCV Id: RCV003787579

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Asp1151Glu
CA346009051
NM_000384.3:c.3453C>G
CA346009052
NM_000384.3:c.3453C>A