Canonical Allele Identifier: PA2741817205
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 2565883
ClinVar RCV Id: RCV003293367

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Ser1969Asn
CA346003724
NM_000384.3:c.5906G>A