Canonical Allele Identifier: PA286586
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 127291

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Gly1294Ala
CA008783
NM_001127511.3:c.3881G>C