Canonical Allele Identifier: PA2825644640
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 236649

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Thr2580Asn
CA049224
NM_001127511.3:c.7739C>A