Canonical Allele Identifier: PA2827969696
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 236626

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Asp1969Val
CA043598
NM_001354898.2:c.5906A>T