Canonical Allele Identifier: PA2825023918
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 809784

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Thr2353Ser
CA16036710
NM_000038.6:c.7057A>T
CA16036712
NM_000038.6:c.7058C>G