Canonical Allele Identifier: PA2827961964
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181819

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Thr2432Ala
CA012961
NM_001354897.2:c.7294A>G