Canonical Allele Identifier: PA2825635873
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1759132

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Ser2497Thr
CA16037620
NM_001127510.3:c.7489T>A