Canonical Allele Identifier: PA658810038
Gene: CDH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 545108
ClinVar RCV Id: RCV000656331
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001783.2:p.Asn692Ser
CA402106923
NM_001792.5:c.2075A>G