Canonical Allele Identifier: PA2827962498
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 630201

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Ala2594Thr
CA049041
NM_001354897.2:c.7780G>A