Canonical Allele Identifier: PA2827028288
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 517399
ClinVar RCV Id: RCV000612806 RCV000786119
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305963.1:p.Ala1067Val
CA362683282
NM_001319034.2:c.3200C>T