Canonical Allele Identifier: PA137809
Gene: DSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 36005
ClinVar RCV Id: RCV000029663 RCV000039419 RCV000157173 RCV000148468 RCV000233024 RCV000776181 RCV000617398 RCV001080880 RCV003944841
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004940.1:p.Leu732Val
CA022624
NM_004949.5:c.2194T>G