Canonical Allele Identifier: PA2580114890
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 2480228
ClinVar RCV Id: RCV004271889
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Ala2475Gly
CA345997186
NM_000384.3:c.7424C>G