Canonical Allele Identifier: PA166467
Gene: CDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 141802
ClinVar RCV Id: RCV000130457 RCV000471390 RCV000656825 RCV001798445 RCV003894994 RCV003993820 RCV003460929
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004351.1:p.Ala817Val
CA166465
NM_004360.5:c.2450C>T