Canonical Allele Identifier: PA2825296152
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 3069319
ClinVar RCV Id: RCV004007863
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008844.1:p.Tyr1430Asn
CA046842
NM_001008844.3:c.4288T>A