Canonical Allele Identifier: PA1139705038
Gene: CDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 921695

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004351.1:p.Asp805Ser
CA1139664744
NM_004360.5:c.2413_2414delinsAG