Canonical Allele Identifier: PA2580114888
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 1960911
ClinVar RCV Id: RCV002715735
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Phe2469Cys
CA345997226
NM_000384.3:c.7406T>G