Canonical Allele Identifier: PA2573237034
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 1441487
ClinVar RCV Id: RCV001979115
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004406.2:p.Asp1046Val
CA037256
NM_004415.4:c.3137A>T