Canonical Allele Identifier: PA133968
Gene: DSG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 44318
ClinVar RCV Id: RCV000254127 RCV000037306 RCV000623308 RCV000472133 RCV000755253 RCV000777969
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001934.2:p.Leu15Gln
CA022107
NM_001943.5:c.44T>A