Canonical Allele Identifier: PA2826966270
Gene: CDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 186668
ClinVar RCV Id: RCV000166300
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304115.1:p.Ser138Arg
CA195505
NM_001317186.2:c.414T>G
CA396471112
NM_001317186.2:c.412A>C
CA396471126
NM_001317186.2:c.414T>A