Canonical Allele Identifier: PA2825636179
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 827302

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Thr2626Ala
CA049327
NM_001127510.3:c.7876A>G