Canonical Allele Identifier: PA915964269
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 523738
ClinVar RCV Id: RCV000627192 RCV002491345
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Met3421Thr
CA042900
NM_000384.3:c.10262T>C