Canonical Allele Identifier: PA2573219250
Gene: DSG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1372646
ClinVar RCV Id: RCV001874722
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001934.2:p.Thr1099Ser
CA402149310
NM_001943.5:c.3295A>T
CA402149314
NM_001943.5:c.3296C>G