Canonical Allele Identifier: PA2825015002
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1770469
ClinVar RCV Id: RCV002387817
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Ala449Ser
CA16024250
NM_000038.6:c.1345G>T