Canonical Allele Identifier: PA299000
Gene: CDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 182400

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004351.1:p.Ala541Val
CA298998
NM_004360.5:c.1622C>T