Canonical Allele Identifier: PA2827986881
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 655278

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Glu1632Gly
CA16032310
NM_001354900.2:c.4895A>G