Canonical Allele Identifier: PA2827959129
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 577215

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Thr1566Ala
CA16031562
NM_001354897.2:c.4696A>G