Canonical Allele Identifier: PA1139702615
Gene: CDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 964177
ClinVar RCV Id: RCV001238353 RCV002436938
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004351.1:p.Phe98Leu
CA396457321
NM_004360.5:c.292T>C
CA396457326
NM_004360.5:c.294C>A
CA396457327
NM_004360.5:c.294C>G