Canonical Allele Identifier: PA1139700390
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 859879
ClinVar RCV Id: RCV001066084 RCV001180414 RCV002402457 RCV003442192
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004406.2:p.Gly2568Ser
CA050483
NM_004415.4:c.7702G>A