Canonical Allele Identifier: PA2573237397
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 1500153

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004406.2:p.Tyr1871Asp
CA045361
NM_004415.4:c.5611T>G