Canonical Allele Identifier: PA2825297101
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 923846
ClinVar RCV Id: RCV001184863

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008844.1:p.Asp2188Val
CA362694997
NM_001008844.3:c.6563A>T