Canonical Allele Identifier: PA915964626
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 128419
ClinVar RCV Id: RCV000116383 RCV000203110 RCV000771061 RCV001094658 RCV001837454 RCV002381423 RCV003477497
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Ala4481Thr
CA022792
NM_000384.3:c.13441G>A