Canonical Allele Identifier: PA298982
Gene: CDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 132709
ClinVar RCV Id: RCV000119150 RCV000160387 RCV000507875 RCV002483202 RCV003328182 RCV003460841
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004351.1:p.Gly239Arg
CA298980
NM_004360.5:c.715G>A
CA396458446
NM_004360.5:c.715G>C