Canonical Allele Identifier: PA2828027690
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 537425

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Thr2255Ser
CA16036727
NM_001354903.2:c.6763A>T
CA16036729
NM_001354903.2:c.6764C>G