Canonical Allele Identifier: PA2827027282
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 228652
ClinVar RCV Id: RCV000221921

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305963.1:p.Ser299Gly
CA10576693
NM_001319034.2:c.895A>G