Canonical Allele Identifier: PA2826965261
Gene: CDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 857052
ClinVar Variation Id: 1503604
ClinVar RCV Id: RCV002045469

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304114.1:p.Ser322Arg
CA396472246
NM_001317185.2:c.964A>C
CA396472258
NM_001317185.2:c.966C>A
CA396472260
NM_001317185.2:c.966C>G