Canonical Allele Identifier: PA2827999072
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411551

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Thr2564Ala
CA16038426
NM_001354901.2:c.7690A>G