Canonical Allele Identifier: PA2580115178
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 1761355
ClinVar RCV Id: RCV002416859
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Glu4181Asp
CA050526
NM_000384.3:c.12543A>C
CA345971016
NM_000384.3:c.12543A>T