Canonical Allele Identifier: PA2825644184
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1356107
ClinVar RCV Id: RCV003772477

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Ser2431Arg
CA16037325
NM_001127511.3:c.7291A>C
CA16037331
NM_001127511.3:c.7293C>A
CA16037332
NM_001127511.3:c.7293C>G