Canonical Allele Identifier: PA2828041955
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 632641

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Ser1532Thr
CA16032217
NM_001354904.2:c.4595G>C