Canonical Allele Identifier: PA2827029949
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 2138916
ClinVar RCV Id: RCV003066461

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305963.1:p.Ala2362Val
CA052251
NM_001319034.2:c.7085C>T