Canonical Allele Identifier: PA168114
Gene: CDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 142338
ClinVar RCV Id: RCV000131408 RCV001036450
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004351.1:p.Tyr797Cys
CA168112
NM_004360.5:c.2390A>G