Canonical Allele Identifier: PA2827947778
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 492672

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Ala2576Thr
CA16038108
NM_001354895.2:c.7726G>A