Canonical Allele Identifier: PA2499267629
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 1044791
ClinVar RCV Id: RCV001349095
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004406.2:p.Ala1274Ser
CA362684926
NM_004415.4:c.3820G>T