Canonical Allele Identifier: PA2826961830
Gene: CDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 463727

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304113.1:p.Thr501Ser
CA396465371
NM_001317184.2:c.1501A>T