Canonical Allele Identifier: PA915963628
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 265883
ClinVar RCV Id: RCV000256248 RCV001837812
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Asp610Gly
CA10588886
NM_000384.3:c.1829A>G