Canonical Allele Identifier: PA2741817440
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 2930903
ClinVar RCV Id: RCV003782165
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Ile4194Val
CA050607
NM_000384.3:c.12580A>G