Canonical Allele Identifier: PA303897
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 199893
ClinVar RCV Id: RCV000181332 RCV003996655 RCV001069898
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004406.2:p.Thr1930Arg
CA006614
NM_004415.4:c.5789C>G