Canonical Allele Identifier: PA2825297114
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 2151665
ClinVar RCV Id: RCV003061457
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008844.1:p.Asp2197Gly
CA362695053
NM_001008844.3:c.6590A>G