Canonical Allele Identifier: PA2828006038
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 233890

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Thr1220Ile
CA10578369
NM_001354905.2:c.3659C>T