Canonical Allele Identifier: PA2499231971
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 1026267
ClinVar RCV Id: RCV001838488 RCV003169534
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Tyr4497Asp
CA345967297
NM_000384.3:c.13489T>G