Canonical Allele Identifier: PA164229
Gene: CDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 141016
ClinVar RCV Id: RCV000129335 RCV000506194 RCV000545072 RCV003317096
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004351.1:p.Ala788Val
CA164227
NM_004360.5:c.2363C>T