Canonical Allele Identifier: PA2828028146
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1356107
ClinVar RCV Id: RCV003772477
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Ser2166Arg
CA16037325
NM_001354906.2:c.6496A>C
CA16037331
NM_001354906.2:c.6498C>A
CA16037332
NM_001354906.2:c.6498C>G