Canonical Allele Identifier: PA157965
Gene: CDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 127922
ClinVar RCV Id: RCV000115851 RCV000120504 RCV000206674 RCV000487740 RCV001798345 RCV003328175 RCV003905101
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004351.1:p.Asp777Asn
CA157963
NM_004360.5:c.2329G>A