Canonical Allele Identifier: PA1139717765
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 919517
ClinVar RCV Id: RCV001177753

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004406.2:p.Gly1182Arg
CA362684305
NM_004415.4:c.3544G>C