Canonical Allele Identifier: PA2825637658
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1368868

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Thr279Ile
CA16023266
NM_001127511.3:c.836C>T