Canonical Allele Identifier: PA280992
Gene: CDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 18453

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004351.1:p.Glu336Asp
CA280990
NM_004360.5:c.1008G>T
CA396459903
NM_004360.5:c.1008G>C