Canonical Allele Identifier: PA658803902
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 537425

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Thr2356Ser
CA16036727
NM_001127510.3:c.7066A>T
CA16036729
NM_001127510.3:c.7067C>G