Canonical Allele Identifier: PA2827029568
Gene: DSP HGNC NCBI

Linked Data

ClinVar Variation Id: 925005
ClinVar RCV Id: RCV001186739 RCV004008628
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305963.1:p.Phe2101Leu
CA362693434
NM_001319034.2:c.6301T>C
CA362693438
NM_001319034.2:c.6303T>A
CA362693439
NM_001319034.2:c.6303T>G