Canonical Allele Identifier: PA2825024535
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482240
ClinVar Variation Id: 642835

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Thr2514Ser
CA048379
NM_000038.6:c.7541C>G
CA16037721
NM_000038.6:c.7540A>T