Canonical Allele Identifier: PA2826960083
Gene: CDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1761701
ClinVar RCV Id: RCV002419273

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304113.1:p.Phe267Leu
CA396458827
NM_001317184.2:c.799T>C
CA396458841
NM_001317184.2:c.801T>A
CA396458844
NM_001317184.2:c.801T>G