Canonical Allele Identifier: PA294387
Gene: CDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 136063

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004351.1:p.Asn674Tyr
CA294385
NM_004360.5:c.2020A>T