Canonical Allele Identifier: PA277888
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 137173
ClinVar RCV Id: RCV000202956 RCV000172750 RCV000400542 RCV000342233 RCV001080914 RCV001095160 RCV000247844 RCV001812025 RCV002492463 RCV000770253 RCV000853001
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004406.2:p.Ile2869Val
CA007748
NM_004415.4:c.8605A>G