Canonical Allele Identifier: PA2827028783
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 2938816

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305963.1:p.Ser1445Arg
CA362689128
NM_001319034.2:c.4333A>C
CA362689134
NM_001319034.2:c.4335T>A
CA362689135
NM_001319034.2:c.4335T>G