Canonical Allele Identifier: PA2825295688
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 2097778
ClinVar RCV Id: RCV003006445

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008844.1:p.Asn1055Asp
CA362683178
NM_001008844.3:c.3163A>G