Canonical Allele Identifier: PA317018
Gene: PRRT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 206682
ClinVar RCV Id: RCV000467192
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_660282.2:p.Ser5Thr
CA317017
NM_145239.3:c.14G>C