Canonical Allele Identifier: PA166619
Gene: CDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 141854
ClinVar RCV Id: RCV000130539 RCV000233909 RCV001283957 RCV003328216 RCV003390820
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004351.1:p.Thr562Ala
CA166617
NM_004360.5:c.1684A>G