Canonical Allele Identifier: PA2741817063
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 2580624
ClinVar RCV Id: RCV003329819
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Ala1133Ser
CA346009170
NM_000384.3:c.3397G>T