Canonical Allele Identifier: PA658669548
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 465917
ClinVar RCV Id: RCV000538707
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004406.2:p.Asn287His
CA362674381
NM_004415.4:c.859A>C