Canonical Allele Identifier: PA915963769
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 404402
ClinVar RCV Id: RCV001837907
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Val1195Met
CA16610626
NM_000384.3:c.3583G>A