Canonical Allele Identifier: PA2825295690
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 3073609
ClinVar RCV Id: RCV004016615

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008844.1:p.Lys1056Gln
CA362683187
NM_001008844.3:c.3166A>C