Canonical Allele Identifier: PA2827986140
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 135702

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Thr1404Ala
CA009444
NM_001354900.2:c.4210A>G