Canonical Allele Identifier: PA2827954009
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2452755

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Thr2585Ser
CA16038056
NM_001354896.2:c.7753A>T
CA16038058
NM_001354896.2:c.7754C>G