Canonical Allele Identifier: PA915964243
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 629221
ClinVar RCV Id: RCV002501002 RCV004027257
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Tyr3272Cys
CA345988680
NM_000384.3:c.9815A>G