Canonical Allele Identifier: PA2825296851
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 2057771
ClinVar RCV Id: RCV002914945
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008844.1:p.Phe2024Cys
CA362693952
NM_001008844.3:c.6071T>G