Canonical Allele Identifier: PA916041549
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 492672

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Ala2594Thr
CA16038108
NM_001354896.2:c.7780G>A