Canonical Allele Identifier: PA916013659
Gene: CDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 640183

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004351.1:p.Trp20Ser
CA396451633
NM_004360.5:c.59G>C