Allele Registry

Canonical Allele Identifier: PA2826965162

Gene: CDH1 HGNC NCBI

ClinVar Variation Id: 569129

HGVS (amino-acid)	Matching Registered Transcripts
NP_001304114.1:p.Phe294Leu	CA396471341 NM_001317185.2:c.880T>C CA396471353 NM_001317185.2:c.882T>A CA396471357 NM_001317185.2:c.882T>G