Canonical Allele Identifier: PA2828012253
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470101

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Ser2461Cys
CA16037960
NM_001354902.2:c.7381A>T