Canonical Allele Identifier: PA168357
Gene: CDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 142437
ClinVar RCV Id: RCV000131558 RCV000205207 RCV000484196 RCV001354689
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004351.1:p.Val794Ile
CA168355
NM_004360.5:c.2380G>A