Canonical Allele Identifier: PA915964241
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 334109
ClinVar RCV Id: RCV000319890 RCV000845467 RCV000356037 RCV002374567 RCV002521387 RCV003114493
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Gly3271Ser
CA066862
NM_000384.3:c.9811G>A