Canonical Allele Identifier: PA2828038828
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 186133

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Ile1178Val
CA008754
NM_001354904.2:c.3532A>G