Canonical Allele Identifier: PA1139702628
Gene: CDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 948093
ClinVar RCV Id: RCV001219280 RCV002322060
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004351.1:p.Phe110Leu
CA396457397
NM_004360.5:c.328T>C
CA396457402
NM_004360.5:c.330T>A
CA396457403
NM_004360.5:c.330T>G