Canonical Allele Identifier: PA2825296001
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 465899
ClinVar RCV Id: RCV000532517 RCV003532171
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008844.1:p.Arg1316Cys
CA362689320
NM_001008844.3:c.3946C>T