ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA100201
Gene: PRRT2
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000024176
RCV002281719
RCV003593864
ClinVar Variation:
31177
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_660282.2:p.Arg266Trp
CA259999
NM_145239.3:c.796C>T