Canonical Allele Identifier: PA2826965294
Gene: CDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 821441
ClinVar RCV Id: RCV001015857
ClinVar Variation Id: 849990

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304114.1:p.Ser328Gly
CA396472322
NM_001317185.2:c.982A>G
CA916081852
NM_001317185.2:c.981_982delinsAG