Canonical Allele Identifier: PA2825295692
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 1728449
ClinVar RCV Id: RCV002322652
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008844.1:p.Leu1058Val
CA362683214
NM_001008844.3:c.3172C>G