Canonical Allele Identifier: PA2828028267
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1356107
ClinVar RCV Id: RCV003772477

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Ser2348Arg
CA16037325
NM_001354903.2:c.7042A>C
CA16037331
NM_001354903.2:c.7044C>A
CA16037332
NM_001354903.2:c.7044C>G