Canonical Allele Identifier: PA2827977062
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 186279

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Thr1417Ile
CA009453
NM_001354899.2:c.4250C>T