Canonical Allele Identifier: PA2499267743
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 1175027
ClinVar RCV Id: RCV001529681 RCV003771639
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004406.2:p.Gly2020Ala
CA362689996
NM_004415.4:c.6059G>C