Canonical Allele Identifier: PA133960
Gene: DSG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 44314
ClinVar RCV Id: RCV000037302 RCV000622126 RCV000771829 RCV001082544 RCV000845296 RCV002496585 RCV003996321 RCV003924917
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001934.2:p.Thr1099Ala
CA022065
NM_001943.5:c.3295A>G