Canonical Allele Identifier: PA2828028737
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 487041

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Pro2257Ala
CA16037879
NM_001354906.2:c.6769C>G