Canonical Allele Identifier: PA2827027362
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 1718022
ClinVar RCV Id: RCV002299568
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305963.1:p.Thr353Ser
CA362675495
NM_001319034.2:c.1057A>T
CA362675498
NM_001319034.2:c.1058C>G