Canonical Allele Identifier: PA2825296105
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 199897
ClinVar RCV Id: RCV000181336 RCV000794685 RCV001189664 RCV002354471 RCV003996657
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008844.1:p.Leu1396Ser
CA006678
NM_001008844.3:c.4187T>C