Canonical Allele Identifier: PA915964652
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 334068
ClinVar RCV Id: RCV000259285 RCV001136660
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Thr4530Ile
CA10612288
NM_000384.3:c.13589C>T