Canonical Allele Identifier: PA168679
Gene: CDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 142546

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004351.1:p.Val132Ile
CA168677
NM_004360.5:c.394G>A