Canonical Allele Identifier: PA349828
Gene: CDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 220695

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004351.1:p.Arg868Cys
CA349826
NM_004360.5:c.2602C>T