Canonical Allele Identifier: PA2827948131
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 132756

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Pro2680Ala
CA014255
NM_001354895.2:c.8038C>G