Canonical Allele Identifier: PA2825294897
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 629400
ClinVar RCV Id: RCV000774106 RCV002501004 RCV003227859 RCV003768364 RCV004027264
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008844.1:p.Ser442Ala
CA027687
NM_001008844.3:c.1324T>G