Allele Registry

Canonical Allele Identifier: PA2580114684

Gene: APOB HGNC NCBI

ClinVar RCV:

RCV002330055

RCV003775854

ClinVar Variation:

1739280

HGVS (amino-acid)	Matching Registered Transcripts
NP_000375.3:p.Ser1425Phe	CA060801 NM_000384.3:c.4274C>T