Canonical Allele Identifier: PA2827027498
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 2165106
ClinVar RCV Id: RCV003088373

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305963.1:p.Pro453Thr
CA362676550
NM_001319034.2:c.1357C>A