Canonical Allele Identifier: PA2827027233
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 2936960
ClinVar RCV Id: RCV003791150

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305963.1:p.Arg265Ser
CA362673996
NM_001319034.2:c.795G>T
CA362673998
NM_001319034.2:c.795G>C