Canonical Allele Identifier: PA2828048773
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 41516

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Ser2495Cys
CA014123
NM_001354904.2:c.7484C>G