Canonical Allele Identifier: PA2580231186
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1719948

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Asp973Val
CA16028781
NM_001354905.2:c.2918A>T