Canonical Allele Identifier: PA2827980045
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 809784

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Thr2325Ser
CA16036710
NM_001354899.2:c.6973A>T
CA16036712
NM_001354899.2:c.6974C>G