Canonical Allele Identifier: PA2580114763
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 1809710
ClinVar RCV Id: RCV002505925
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Ile1839Thr
CA346004552
NM_000384.3:c.5516T>C