Canonical Allele Identifier: PA2826394311
Gene: PRRT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 206689

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243371.1:p.Pro216His
CA317031
NM_001256442.2:c.647C>A