Canonical Allele Identifier: PA2828030113
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1063812
ClinVar RCV Id: RCV003652229
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Pro2464Ser
CA16039214
NM_001354906.2:c.7390C>T