Canonical Allele Identifier: PA2826963170
Gene: CDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1790622
ClinVar RCV Id: RCV002450207
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304113.1:p.Pro738Leu
CA396471197
NM_001317184.2:c.2213C>T