Canonical Allele Identifier: PA2827976597
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 186133

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Ile1276Val
CA008754
NM_001354899.2:c.3826A>G