Canonical Allele Identifier: PA2828028408
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2159583
ClinVar RCV Id: RCV003653655
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Ser2204Phe
CA048129
NM_001354906.2:c.6611C>T