Canonical Allele Identifier: PA2826965020
Gene: CDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1021161
ClinVar RCV Id: RCV001320871

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304114.1:p.Asp261Val
CA396470917
NM_001317185.2:c.782A>T