Canonical Allele Identifier: PA2826961729
Gene: CDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 463725
ClinVar RCV Id: RCV000534032

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304113.1:p.Leu487Val
CA396465185
NM_001317184.2:c.1459C>G