Canonical Allele Identifier: PA133906
Gene: DSG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 16818
ClinVar RCV Id: RCV000018311 RCV000018312 RCV000037270 RCV000157180 RCV000148471 RCV000157179 RCV000243248 RCV000757183 RCV000769508 RCV000852739 RCV003944829
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001934.2:p.Val56Met
CA021523
NM_001943.5:c.166G>A