Canonical Allele Identifier: PA916015120
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_004351.1:p.Ser844Gly
CA396472322
NM_004360.5:c.2530A>G
CA916081852
NM_004360.5:c.2529_2530delinsAG