Canonical Allele Identifier: PA2825147134
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 3231387
ClinVar RCV Id: RCV004525458
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Thr840Ser
CA346011098
NM_000384.3:c.2519C>G
CA346011100
NM_000384.3:c.2518A>T