Canonical Allele Identifier: PA915964040
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 490400
ClinVar RCV Id: RCV000581160 RCV004024626 RCV004017684
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Lys2428Arg
CA345997492
NM_000384.3:c.7283A>G