Canonical Allele Identifier: PA1139682830
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 265896
ClinVar RCV Id: RCV000256307 RCV001283874 RCV001837820 RCV002248497 RCV002379100 RCV000845480
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Gln4494del
CA1546518
NM_000384.3:c.13480_13482del