Canonical Allele Identifier: PA2828032173
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 135729

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Ser270Gly
CA015623
NM_001354904.2:c.808A>G