Canonical Allele Identifier: PA2826394060
Gene: PRRT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2831859
ClinVar RCV Id: RCV003758285

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243371.1:p.Ala2Glu
CA7994459
NM_001256442.2:c.5C>A