Canonical Allele Identifier: PA2580312007
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 2151665
ClinVar RCV Id: RCV003061457

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004406.2:p.Asp2796Gly
CA362695053
NM_004415.4:c.8387A>G