Canonical Allele Identifier: PA915964639
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 627679
ClinVar RCV Id: RCV002386333 RCV002533985
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Ser4517Phe
CA053161
NM_000384.3:c.13550C>T