Canonical Allele Identifier: PA2828029383
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 41516

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Ser2520Cys
CA014123
NM_001354903.2:c.7559C>G