Canonical Allele Identifier: PA2825297130
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 2186899
ClinVar RCV Id: RCV002611188
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008844.1:p.Ala2207Val
CA362695106
NM_001008844.3:c.6620C>T