Canonical Allele Identifier: PA2825296579
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 3070945
ClinVar RCV Id: RCV004014447

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008844.1:p.Asn1799Lys
CA362692444
NM_001008844.3:c.5397T>A
CA362692445
NM_001008844.3:c.5397T>G