Canonical Allele Identifier: PA2825635982
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1447119
ClinVar RCV Id: RCV002563486
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Ser2557Thr
CA16037990
NM_001127510.3:c.7669T>A