Canonical Allele Identifier: PA2825296049
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 3071540
ClinVar RCV Id: RCV004016034

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008844.1:p.Pro1347Leu
CA362689520
NM_001008844.3:c.4040C>T