Canonical Allele Identifier: PA2825297119
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 1041718
ClinVar RCV Id: RCV001345565 RCV001526067 RCV004005199
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008844.1:p.Thr2199Ser
CA133977951
NM_001008844.3:c.6595A>T
CA362695063
NM_001008844.3:c.6596C>G