Canonical Allele Identifier: PA2825297226
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 2502078

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008844.1:p.Asn2256Lys
CA362695389
NM_001008844.3:c.6768T>A
CA362695390
NM_001008844.3:c.6768T>G