Canonical Allele Identifier: PA2825023929
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 537425

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Thr2356Ser
CA16036727
NM_000038.6:c.7066A>T
CA16036729
NM_000038.6:c.7067C>G