Canonical Allele Identifier: PA2825644716
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 827303

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Thr2608Ser
CA16038447
NM_001127511.3:c.7822A>T
CA16038449
NM_001127511.3:c.7823C>G