Canonical Allele Identifier: PA1139722478
Gene: DSG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 948689
ClinVar RCV Id: RCV001219995
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001934.2:p.Val933Leu
CA402146777
NM_001943.5:c.2797G>T
CA402146778
NM_001943.5:c.2797G>C