ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA317047
Gene: PRRT2
HGNC
NCBI
Linked Data
ClinVar Variation Id:
206697
ClinVar RCV Id:
RCV000188781
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_660282.2:p.Met11Arg
CA317046
NM_145239.3:c.32T>G