Canonical Allele Identifier: PA2828002520
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 140839

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Cys1487Gly
CA009712
NM_001354902.2:c.4459T>G