Canonical Allele Identifier: PA2573237593
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 1402267
ClinVar RCV Id: RCV001906351

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004406.2:p.Tyr2528Asp
CA362693329
NM_004415.4:c.7582T>G