Canonical Allele Identifier: PA193527
Gene: CDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 185969

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004351.1:p.Leu791Phe
CA193525
NM_004360.5:c.2371C>T