Canonical Allele Identifier: PA915963963
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 575116
ClinVar RCV Id: RCV001838103
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Thr1941Ile
CA062516
NM_000384.3:c.5822C>T