Canonical Allele Identifier: PA916041542
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 573707

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Ser2587Arg
CA16038066
NM_001354896.2:c.7759A>C
CA16038072
NM_001354896.2:c.7761T>A
CA16038073
NM_001354896.2:c.7761T>G