Canonical Allele Identifier: PA2825297142
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 2945289
ClinVar RCV Id: RCV003800943
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008844.1:p.Leu2214Ser
CA362695146
NM_001008844.3:c.6641T>C