Canonical Allele Identifier: PA2827980748
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2452755

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Thr2539Ser
CA16038056
NM_001354899.2:c.7615A>T
CA16038058
NM_001354899.2:c.7616C>G