Canonical Allele Identifier: PA2826963449
Gene: CDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2846498
ClinVar RCV Id: RCV003625764

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304113.1:p.Ser783Arg
CA396472320
NM_001317184.2:c.2347A>C
CA396472329
NM_001317184.2:c.2349T>A
CA396472330
NM_001317184.2:c.2349T>G