Canonical Allele Identifier: PA2827026884
Gene: DSP HGNC NCBI
ClinVar RCV:
RCV001886827
ClinVar Variation:
1388757
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305963.1:p.Ser32Gly
CA362675780
NM_001319034.2:c.94A>G