Canonical Allele Identifier: PA2828001970
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 186133

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Ile1213Val
CA008754
NM_001354902.2:c.3637A>G