Canonical Allele Identifier: PA2828006707
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 487051
ClinVar RCV Id: RCV000567763
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Ser1421Phe
CA16031733
NM_001354905.2:c.4262C>T