Canonical Allele Identifier: PA354026
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 222583

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004406.2:p.Thr2287Ser
CA354024
NM_004415.4:c.6859A>T
CA362691716
NM_004415.4:c.6860C>G