Canonical Allele Identifier: PA2580311897
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 2057771
ClinVar RCV Id: RCV002914945
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004406.2:p.Phe2623Cys
CA362693952
NM_004415.4:c.7868T>G