Canonical Allele Identifier: PA2825296098
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 573062
ClinVar RCV Id: RCV000694629 RCV001191951 RCV002477576 RCV003999620 RCV004025209
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008844.1:p.Asp1388Asn
CA046150
NM_001008844.3:c.4162G>A