Canonical Allele Identifier: PA2825294653
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 2936960
ClinVar RCV Id: RCV003791150

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008844.1:p.Arg265Ser
CA362673996
NM_001008844.3:c.795G>T
CA362673998
NM_001008844.3:c.795G>C