Canonical Allele Identifier: PA2827978715
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1171348

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Thr1919Ile
CA16034105
NM_001354899.2:c.5756C>T