Canonical Allele Identifier: PA2827029714
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 2025955
ClinVar RCV Id: RCV002858247

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305963.1:p.Ala2212Ser
CA051243
NM_001319034.2:c.6634G>T