Canonical Allele Identifier: PA286636
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 127307

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Ala1861Ser
CA010547
NM_001127511.3:c.5581G>T