Canonical Allele Identifier: PA2825019510
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 418012

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Ile1254Val
CA036589
NM_000038.6:c.3760A>G