Canonical Allele Identifier: PA298967
Gene: CDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 182390

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004351.1:p.Arg90Trp
CA298965
NM_004360.5:c.268C>T