Canonical Allele Identifier: PA2826963235
Gene: CDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 569129
ClinVar RCV Id: RCV000689679
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304113.1:p.Phe749Leu
CA396471341
NM_001317184.2:c.2245T>C
CA396471353
NM_001317184.2:c.2247T>A
CA396471357
NM_001317184.2:c.2247T>G