Canonical Allele Identifier: PA2826965090
Gene: CDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 186668
ClinVar RCV Id: RCV000166300

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304114.1:p.Ser277Arg
CA195505
NM_001317185.2:c.831T>G
CA396471112
NM_001317185.2:c.829A>C
CA396471126
NM_001317185.2:c.831T>A