Canonical Allele Identifier: PA121990
Gene: CDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 12231

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004351.1:p.Leu711Val
CA121988
NM_004360.5:c.2131C>G