Canonical Allele Identifier: PA2830271269
Gene: PRRT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3219733
ClinVar RCV Id: RCV004510554
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_660282.2:p.Asn212Thr
CA395479135
NM_145239.3:c.635A>C