Canonical Allele Identifier: PA2580114761
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 1747771
ClinVar RCV Id: RCV002349823
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Asn1826Lys
CA346004640
NM_000384.3:c.5478C>G
CA346004641
NM_000384.3:c.5478C>A