Canonical Allele Identifier: PA2827029910
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 3075276
ClinVar RCV Id: RCV004015802

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305963.1:p.Thr2332Ser
CA362694915
NM_001319034.2:c.6994A>T
CA362694917
NM_001319034.2:c.6995C>G