Canonical Allele Identifier: PA2825296013
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 572493
ClinVar RCV Id: RCV000693885

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008844.1:p.Glu1324Gln
CA362689370
NM_001008844.3:c.3970G>C