Canonical Allele Identifier: PA2826960037
Gene: CDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 481689
ClinVar RCV Id: RCV001233599 RCV000571849
ClinVar Variation Id: 491557
ClinVar RCV Id: RCV000584658
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304113.1:p.Thr263Ser
CA396458753
NM_001317184.2:c.787A>T
CA396458763
NM_001317184.2:c.788C>G