Canonical Allele Identifier: PA2825295979
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 3073499
ClinVar RCV Id: RCV004016505 RCV004371979
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008844.1:p.Arg1297Thr
CA045561
NM_001008844.3:c.3890G>C