Canonical Allele Identifier: PA1139701410
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 922338

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004406.2:p.Arg2791Cys
CA133977876
NM_004415.4:c.8371C>T