Canonical Allele Identifier: PA298997
Gene: CDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 182399
ClinVar RCV Id: RCV000160393 RCV000212373 RCV000234355 RCV001356277
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004351.1:p.Pro537Leu
CA298995
NM_004360.5:c.1610C>T