Canonical Allele Identifier: PA2830271186
Gene: PRRT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 839697
ClinVar RCV Id: RCV001041514 RCV002320251
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_660282.2:p.Ala135_Pro142del
CA7994521
NM_145239.3:c.404_427del