Canonical Allele Identifier: PA2828024884
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411472

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Gly1820Ser
CA16033936
NM_001354903.2:c.5458G>A