Canonical Allele Identifier: PA354033
Gene: DSG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 222567
ClinVar RCV Id: RCV000208481
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001934.2:p.Phe888Leu
CA046776
NM_001943.5:c.2664C>A
CA402145954
NM_001943.5:c.2662T>C
CA402145961
NM_001943.5:c.2664C>G