Canonical Allele Identifier: PA303967
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 199939

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004406.2:p.Val2107Leu
CA006855
NM_004415.4:c.6319G>C