Canonical Allele Identifier: PA2827028855
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 3072235
ClinVar RCV Id: RCV004012265

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305963.1:p.Glu1495Gln
CA362689464
NM_001319034.2:c.4483G>C