Canonical Allele Identifier: PA915964573
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 334073
ClinVar RCV Id: RCV000297805 RCV000403295
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Tyr4328Cys
CA10614122
NM_000384.3:c.12983A>G