Canonical Allele Identifier: PA2825295691
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 3085985
ClinVar RCV Id: RCV004377305
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008844.1:p.Lys1056Thr
CA362683193
NM_001008844.3:c.3167A>C