Canonical Allele Identifier: PA2826963362
Gene: CDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 216594
ClinVar Variation Id: 2775047
ClinVar RCV Id: RCV003585095

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304113.1:p.Phe772Leu
CA336541
NM_001317184.2:c.2314T>C
CA396472171
NM_001317184.2:c.2316T>A
CA396472173
NM_001317184.2:c.2316T>G