Canonical Allele Identifier: PA2827029978
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 191646
ClinVar RCV Id: RCV000171924 RCV000618112 RCV001088341 RCV001160406 RCV001160407 RCV001160408 RCV001183474
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305963.1:p.Ser2378Leu
CA007566
NM_001319034.2:c.7133C>T