Canonical Allele Identifier: PA1139682923
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 919908
ClinVar RCV Id: RCV001178365 RCV002067888 RCV004033021
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Gly4557Ala
CA053453
NM_000384.3:c.13670G>C