Canonical Allele Identifier: PA2828013078
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 41516

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Ser2461Cys
CA014123
NM_001354905.2:c.7382C>G