Canonical Allele Identifier: PA2827985519
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 418012

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Ile1213Val
CA036589
NM_001354900.2:c.3637A>G