Canonical Allele Identifier: PA191701
Gene: CDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 185349
ClinVar RCV Id: RCV000164755
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004351.1:p.Thr544Ser
CA191699
NM_004360.5:c.1630A>T
CA396465147
NM_004360.5:c.1631C>G