Canonical Allele Identifier: PA2828049629
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 135724

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Ile2630Val
CA014501
NM_001354904.2:c.7888A>G