Canonical Allele Identifier: PA2825644335
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1759132

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Ser2479Thr
CA16037620
NM_001127511.3:c.7435T>A