Allele Registry

Canonical Allele Identifier: PA1139674325

Gene: APOB HGNC NCBI

ClinVar Allele:

908447

ClinVar RCV:

RCV001875825

RCV002261297

RCV002436736

ClinVar Variation:

918926

HGVS (amino-acid)	Matching Registered Transcripts
NP_000375.3:p.Pro955Leu	CA057436 NM_000384.3:c.2864C>T