Canonical Allele Identifier: PA1139700680
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 959843
ClinVar RCV Id: RCV001233265

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004406.2:p.Ser2607Gly
CA362693846
NM_004415.4:c.7819A>G