Canonical Allele Identifier: PA166007
Gene: CDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 141639

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004351.1:p.Gly62Ser
CA166005
NM_004360.5:c.184G>A