Canonical Allele Identifier: PA2828029068
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 573707

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Ser2468Arg
CA16038066
NM_001354903.2:c.7402A>C
CA16038072
NM_001354903.2:c.7404T>A
CA16038073
NM_001354903.2:c.7404T>G