Canonical Allele Identifier: PA157991
Gene: CDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 133855
ClinVar RCV Id: RCV000120515 RCV000160390 RCV000205108 RCV000588122 RCV001358315 RCV002498556 RCV003328189 RCV003492525 RCV003952588
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004351.1:p.Trp409Arg
CA157989
NM_004360.5:c.1225T>C
CA396461389
NM_004360.5:c.1225T>A