Canonical Allele Identifier: PA891857713
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 565929
ClinVar RCV Id: RCV000685612
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004406.2:p.Arg425Leu
CA133956046
NM_004415.4:c.1274G>T