Canonical Allele Identifier: PA2827987792
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1171348

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Thr1906Ile
CA16034105
NM_001354900.2:c.5717C>T