Canonical Allele Identifier: PA165389
Gene: CDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 41786

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004351.1:p.Arg224His
CA165387
NM_004360.5:c.671G>A