Canonical Allele Identifier: PA193928
Gene: CDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 186125

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004351.1:p.Thr568Ile
CA193926
NM_004360.5:c.1703C>T