Canonical Allele Identifier: PA169147
Gene: CDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 142692
ClinVar RCV Id: RCV000132054 RCV000200245 RCV000482830 RCV003328231
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004351.1:p.Arg90Gln
CA169145
NM_004360.5:c.269G>A
CA645596593
NM_004360.5:c.269_270delinsAA