Canonical Allele Identifier: PA915964035
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 412949
ClinVar RCV Id: RCV001837919 RCV003168877
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Ser2408Phe
CA064202
NM_000384.3:c.7223C>T