Canonical Allele Identifier: PA1139671860
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 919669
ClinVar RCV Id: RCV001177981
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Ser72Asn
CA345965013
NM_000384.3:c.215G>A