Canonical Allele Identifier: PA916041519
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 487041

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Pro2558Ala
CA16037879
NM_001354896.2:c.7672C>G