Canonical Allele Identifier: PA2827980644
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 957710

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Ser2507Gly
CA16037848
NM_001354899.2:c.7519A>G