Canonical Allele Identifier: PA1139677260
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 920431

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Tyr2177Ser
CA346001556
NM_000384.3:c.6530A>C