Canonical Allele Identifier: PA2828014527
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1439196

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Ser23Ile
CA16023319
NM_001354906.2:c.68G>T