Canonical Allele Identifier: PA2828006681
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482393

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Ile1412Phe
CA039634
NM_001354905.2:c.4234A>T