Canonical Allele Identifier: PA2573237614
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 1371902
ClinVar RCV Id: RCV001872606
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004406.2:p.Ser2570Gly
CA362693602
NM_004415.4:c.7708A>G