Canonical Allele Identifier: PA2741817448
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 2565865
ClinVar RCV Id: RCV003293357
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Phe4362Leu
CA345969415
NM_000384.3:c.13086T>G
CA345969424
NM_000384.3:c.13086T>A
CA345969431
NM_000384.3:c.13084T>C