Canonical Allele Identifier: PA2828028996
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1496440
ClinVar RCV Id: RCV002625394
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Ser2455Ala
CA16037987
NM_001354903.2:c.7363T>G