Canonical Allele Identifier: PA915963760
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 808691
ClinVar RCV Id: RCV000997066 RCV002550706
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Ser1135Asn
CA058755
NM_000384.3:c.3404G>A