Canonical Allele Identifier: PA2827980357
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1356107
ClinVar RCV Id: RCV003772477

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Ser2421Arg
CA16037325
NM_001354899.2:c.7261A>C
CA16037331
NM_001354899.2:c.7263C>A
CA16037332
NM_001354899.2:c.7263C>G