Canonical Allele Identifier: PA2825295986
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 920297
ClinVar RCV Id: RCV001178967
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008844.1:p.Glu1301Gly
CA362689218
NM_001008844.3:c.3902A>G