Canonical Allele Identifier: PA303901
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 199895
ClinVar RCV Id: RCV000181334 RCV000286712 RCV000391599 RCV000341732 RCV001852270 RCV002354469 RCV003996656 RCV001525481
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004406.2:p.Arg1943Gly
CA006637
NM_004415.4:c.5827A>G