Canonical Allele Identifier: PA2828005579
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 186133

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Ile1144Val
CA008754
NM_001354905.2:c.3430A>G