Canonical Allele Identifier: PA2827995205
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 186279

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Thr1386Ile
CA009453
NM_001354901.2:c.4157C>T