Canonical Allele Identifier: PA2826961698
Gene: CDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 185349
ClinVar RCV Id: RCV000164755
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304113.1:p.Thr483Ser
CA191699
NM_001317184.2:c.1447A>T
CA396465147
NM_001317184.2:c.1448C>G