Canonical Allele Identifier: PA2573062457
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 1327347
ClinVar RCV Id: RCV001787627
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Thr1950Ala
CA346003847
NM_000384.3:c.5848A>G