Canonical Allele Identifier: PA2825296097
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 3072811
ClinVar RCV Id: RCV004013833

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008844.1:p.Asp1388Glu
CA362689790
NM_001008844.3:c.4164C>A
CA362689791
NM_001008844.3:c.4164C>G