Canonical Allele Identifier: PA2827029285
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 222583

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305963.1:p.Thr1844Ser
CA354024
NM_001319034.2:c.5530A>T
CA362691716
NM_001319034.2:c.5531C>G