Canonical Allele Identifier: PA2825295678
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 2949278

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008844.1:p.Asn1048Lys
CA362683101
NM_001008844.3:c.3144C>A
CA362683102
NM_001008844.3:c.3144C>G