Canonical Allele Identifier: PA2573219101
Gene: DSG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1437147
ClinVar RCV Id: RCV001931813
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001934.2:p.Thr645Ser
CA402139470
NM_001943.5:c.1933A>T
CA402139476
NM_001943.5:c.1934C>G