ClinGen Allele Registry
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Canonical Allele Identifier:
PA2827029591
Gene: DSP
HGNC
NCBI
Linked Data
ClinVar Variation Id:
928071
ClinVar RCV Id:
RCV001191722
RCV004033436
RCV003770165
RCV004010540
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001305963.1:p.Gln2113Leu
CA133976393
NM_001319034.2:c.6338A>T