Canonical Allele Identifier: PA2825639676
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411386

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Asp971Gly
CA034127
NM_001127511.3:c.2912A>G