ClinGen Allele Registry
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Canonical Allele Identifier:
PA2827029929
Gene: DSP
HGNC
NCBI
Linked Data
ClinVar Variation Id:
667230
ClinVar RCV Id:
RCV000825919
RCV002434035
RCV003768562
RCV003532286
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001305963.1:p.Arg2348His
CA052149
NM_001319034.2:c.7043G>A