Canonical Allele Identifier: PA349935
Gene: CDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 219925
ClinVar RCV Id: RCV000205814

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004351.1:p.Ser829Tyr
CA349933
NM_004360.5:c.2486C>A