Canonical Allele Identifier: PA2825644921
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 243109

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Val2668Ala
CA049793
NM_001127511.3:c.8003T>C