Canonical Allele Identifier: PA157979
Gene: CDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 133852
ClinVar RCV Id: RCV000120510 RCV000218851 RCV000705105 RCV002260610
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004351.1:p.His97Asp
CA157977
NM_004360.5:c.289C>G