Canonical Allele Identifier: PA1139682268
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 3231374
ClinVar RCV Id: RCV004525445
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Gln4180Lys
CA345971027
NM_000384.3:c.12538C>A