Canonical Allele Identifier: PA298979
Gene: CDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 182394

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004351.1:p.Asn238His
CA298977
NM_004360.5:c.712A>C