Canonical Allele Identifier: PA2828007205
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 632641

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Ser1498Thr
CA16032217
NM_001354905.2:c.4493G>C