Canonical Allele Identifier: PA2828024395
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 236620

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Gly1735Arg
CA042181
NM_001354903.2:c.5203G>A
CA16033377
NM_001354903.2:c.5203G>C