Canonical Allele Identifier: PA2828006623
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 577215

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Thr1396Ala
CA16031562
NM_001354905.2:c.4186A>G