Canonical Allele Identifier: PA2827982476
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1368868

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Thr238Ile
CA16023266
NM_001354900.2:c.713C>T