Canonical Allele Identifier: PA2828031771
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 141927

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Arg191Gly
CA012188
NM_001354904.2:c.571C>G