Canonical Allele Identifier: PA658669481
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 451932
ClinVar RCV Id: RCV000522871 RCV000764657 RCV001170909 RCV001375634 RCV001212813 RCV002384015 RCV003403239 RCV004003635
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004406.2:p.Gly46Asp
CA027812
NM_004415.4:c.137G>A