Canonical Allele Identifier: PA2828049182
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 243109

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Val2560Ala
CA049793
NM_001354904.2:c.7679T>C