Canonical Allele Identifier: PA2825296865
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 1522978
ClinVar RCV Id: RCV002036415

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008844.1:p.Ile2038Met
CA362694047
NM_001008844.3:c.6114A>G