Canonical Allele Identifier: PA2827028276
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 2097778
ClinVar RCV Id: RCV003006445
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305963.1:p.Asn1055Asp
CA362683178
NM_001319034.2:c.3163A>G