Canonical Allele Identifier: PA1139717496
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 957282
ClinVar RCV Id: RCV001230234
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004406.2:p.Lys1064Glu
CA362683256
NM_004415.4:c.3190A>G