Canonical Allele Identifier: PA2580261583
Gene: DSG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1764979
ClinVar RCV Id: RCV002449860
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001934.2:p.Phe296Leu
CA402135567
NM_001943.5:c.886T>C
CA402135576
NM_001943.5:c.888C>A
CA402135577
NM_001943.5:c.888C>G