Canonical Allele Identifier: PA181072
Gene: DSG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 177961
ClinVar RCV Id: RCV000154627 RCV000618561 RCV000771841 RCV000845294 RCV001086616 RCV002478453 RCV003927491 RCV003998257
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001934.2:p.His790Tyr
CA021768
NM_001943.5:c.2368C>T