Canonical Allele Identifier: PA2828012342
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1759132

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Ser2337Thr
CA16037620
NM_001354905.2:c.7009T>A