Canonical Allele Identifier: PA2828012178
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482240
ClinVar Variation Id: 642835

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Thr2423Ser
CA048379
NM_001354902.2:c.7268C>G
CA16037721
NM_001354902.2:c.7267A>T