Canonical Allele Identifier: PA2827989132
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 537425

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Thr2315Ser
CA16036727
NM_001354900.2:c.6943A>T
CA16036729
NM_001354900.2:c.6944C>G