Canonical Allele Identifier: PA2573302490
Gene: PRRT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1466526
ClinVar RCV Id: RCV001979639
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_660282.2:p.Pro144Ser
CA395478661
NM_145239.3:c.430C>T