Canonical Allele Identifier: PA2827947787
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1692381
ClinVar RCV Id: RCV002257176 RCV003774771
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Ser2578Pro
CA16038121
NM_001354895.2:c.7732T>C