Canonical Allele Identifier: PA2573167402
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 1483674
ClinVar RCV Id: RCV001998893
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Glu2458Asp
CA064363
NM_000384.3:c.7374A>T
CA345997295
NM_000384.3:c.7374A>C