Canonical Allele Identifier: PA2828028559
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482396

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Met2390Ile
CA16037587
NM_001354903.2:c.7170G>A
CA16037588
NM_001354903.2:c.7170G>C
CA16037589
NM_001354903.2:c.7170G>T