Canonical Allele Identifier: PA1139722232
Gene: DSG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 918295
ClinVar RCV Id: RCV001175800
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001934.2:p.Asn880Lys
CA402145804
NM_001943.5:c.2640T>A
CA402145805
NM_001943.5:c.2640T>G