Canonical Allele Identifier: PA2580115024
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 1768362
ClinVar RCV Id: RCV002387270
ClinVar Variation Id: 2451335
ClinVar RCV Id: RCV003182351

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Met3280Ile
CA345988549
NM_000384.3:c.9840G>T
CA345988551
NM_000384.3:c.9840G>C
CA345988554
NM_000384.3:c.9840G>A