Canonical Allele Identifier: PA2741817201
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 2502248
ClinVar RCV Id: RCV003228666

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.His1966Gln
CA346003738
NM_000384.3:c.5898C>G
CA346003739
NM_000384.3:c.5898C>A