Canonical Allele Identifier: PA1139704900
Gene: CDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 923471
ClinVar RCV Id: RCV001184180

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004351.1:p.Leu769Ser
CA396470770
NM_004360.5:c.2306T>C