Canonical Allele Identifier: PA915977069
Gene: DSG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 648493
ClinVar RCV Id: RCV000803237
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001934.2:p.Ser712_Met714del
CA044922
NM_001943.5:c.2134_2142del