Canonical Allele Identifier: PA915963436
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 128422
ClinVar RCV Id: RCV000116386 RCV000256320 RCV000771030 RCV001356976 RCV000324495 RCV001094606 RCV001837457 RCV002433606 RCV000845576
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Thr98Ile
CA022817
NM_000384.3:c.293C>T
CA645517693
NM_000384.3:c.293_294delinsTT