Canonical Allele Identifier: PA2827029913
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 2002359
ClinVar RCV Id: RCV002820348

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305963.1:p.Pro2334Leu
CA362694930
NM_001319034.2:c.7001C>T