Canonical Allele Identifier: PA2828012036
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 939283

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Thr2390Ser
CA16037526
NM_001354902.2:c.7168A>T
CA16037528
NM_001354902.2:c.7169C>G