Canonical Allele Identifier: PA913199526
Gene: CDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 629436
ClinVar RCV Id: RCV000774143
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004351.1:p.Phe69Val
CA396457157
NM_004360.5:c.205T>G