Canonical Allele Identifier: PA2828028744
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 156483

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Tyr2416Cys
CA013809
NM_001354903.2:c.7247A>G