Canonical Allele Identifier: PA2573167865
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 1404457

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Thr4212Ser
CA050732
NM_000384.3:c.12635C>G
CA345970807
NM_000384.3:c.12634A>T