Canonical Allele Identifier: PA2828025073
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1171348

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Thr1846Ile
CA16034105
NM_001354903.2:c.5537C>T