Canonical Allele Identifier: PA2825296031
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 393020

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008844.1:p.Tyr1336Cys
CA045770
NM_001008844.3:c.4007A>G