Canonical Allele Identifier: PA2828009370
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 632641

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Ser1567Thr
CA16032217
NM_001354902.2:c.4700G>C