Canonical Allele Identifier: PA285796
Gene: PRRT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 96494
ClinVar RCV Id: RCV000082646 RCV000224146 RCV001082873 RCV002311740 RCV002274919 RCV002505010
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_660282.2:p.Pro216Leu
CA285795
NM_145239.3:c.647C>T