Canonical Allele Identifier: PA2826966616
Gene: CDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 821441
ClinVar RCV Id: RCV001015857
ClinVar Variation Id: 849990

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304115.1:p.Ser189Gly
CA396472322
NM_001317186.2:c.565A>G
CA916081852
NM_001317186.2:c.564_565delinsAG