Canonical Allele Identifier: PA2827966842
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1719948

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Asp1108Val
CA16028781
NM_001354898.2:c.3323A>T