Canonical Allele Identifier: PA1139731692
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 947593
ClinVar RCV Id: RCV003650732
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Ser2742Phe
CA16039069
NM_001354896.2:c.8225C>T