Canonical Allele Identifier: PA167220
Gene: CDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 142040
ClinVar Variation Id: 406646
ClinVar Variation Id: 491524
ClinVar RCV Id: RCV000581517

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004351.1:p.Phe75Leu
CA167218
NM_004360.5:c.223T>C
CA8129813
NM_004360.5:c.225C>A
CA8129814
NM_004360.5:c.225C>G