Canonical Allele Identifier: PA2827028914
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 3072811
ClinVar RCV Id: RCV004013833
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305963.1:p.Asp1544Glu
CA362689790
NM_001319034.2:c.4632C>A
CA362689791
NM_001319034.2:c.4632C>G