Canonical Allele Identifier: PA915963772
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 334152
ClinVar RCV Id: RCV000333253 RCV000385388 RCV002450903 RCV003477899 RCV001837865
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Asp1199Asn
CA059218
NM_000384.3:c.3595G>A