Canonical Allele Identifier: PA1139704362
Gene: CDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 861095
ClinVar RCV Id: RCV001067535
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004351.1:p.Thr539Ser
CA396465074
NM_004360.5:c.1615A>T
CA396465079
NM_004360.5:c.1616C>G