Canonical Allele Identifier: PA915963968
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 572387

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Asp1997Asn
CA062688
NM_000384.3:c.5989G>A