Canonical Allele Identifier: PA2741817199
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 2562187
ClinVar RCV Id: RCV003310247 RCV003777129
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Ser1949Phe
CA062538
NM_000384.3:c.5846C>T