Canonical Allele Identifier: PA2825642540
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411472

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Gly1903Ser
CA16033936
NM_001127511.3:c.5707G>A