Canonical Allele Identifier: PA1139719354
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 920760
ClinVar RCV Id: RCV001179713
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004406.2:p.Arg1951Gly
CA362689548
NM_004415.4:c.5851C>G