Canonical Allele Identifier: PA133936
Gene: DSG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 44304
ClinVar RCV Id: RCV000037289 RCV000463983 RCV000620514 RCV000769516 RCV001528736 RCV002496584 RCV003996317
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001934.2:p.Met863Leu
CA021831
NM_001943.5:c.2587A>C
CA402145314
NM_001943.5:c.2587A>T