Canonical Allele Identifier: PA1139679990
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 925611
ClinVar RCV Id: RCV001284273 RCV002379723 RCV001838409
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Asp3289Glu
CA066909
NM_000384.3:c.9867C>A
CA345988415
NM_000384.3:c.9867C>G