Canonical Allele Identifier: PA286638
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 127307

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Ala1879Ser
CA010547
NM_001127510.3:c.5635G>T