Canonical Allele Identifier: PA2825295695
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 957282
ClinVar RCV Id: RCV001230234

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008844.1:p.Lys1064Glu
CA362683256
NM_001008844.3:c.3190A>G