Canonical Allele Identifier: PA2825640878
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 233890

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Thr1362Ile
CA10578369
NM_001127511.3:c.4085C>T