Canonical Allele Identifier: PA2828051909
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 925531

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Ser237Thr
CA16023258
NM_001354905.2:c.710G>C