Canonical Allele Identifier: PA2827994079
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 823620

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Thr1053Ala
CA035066
NM_001354901.2:c.3157A>G