Canonical Allele Identifier: PA2580311997
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 1720208
ClinVar RCV Id: RCV002298002 RCV003533158
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004406.2:p.Leu2781Ser
CA362694955
NM_004415.4:c.8342T>C