Canonical Allele Identifier: PA2827962046
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1356107
ClinVar RCV Id: RCV003772477

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Ser2459Arg
CA16037325
NM_001354897.2:c.7375A>C
CA16037331
NM_001354897.2:c.7377C>A
CA16037332
NM_001354897.2:c.7377C>G