Canonical Allele Identifier: PA1139700295
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 923585
ClinVar RCV Id: RCV001184404

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004406.2:p.Val2517Leu
CA050074
NM_004415.4:c.7549G>T
CA362693260
NM_004415.4:c.7549G>C