Canonical Allele Identifier: PA2827971422
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1059095

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Asp2494Gly
CA16037756
NM_001354898.2:c.7481A>G