Canonical Allele Identifier: PA915963457
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 265874
ClinVar RCV Id: RCV000256242 RCV000776489 RCV001837810
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Ile135Val
CA060400
NM_000384.3:c.403A>G