Canonical Allele Identifier: PA2828028967
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470101

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Ser2451Cys
CA16037960
NM_001354903.2:c.7351A>T