Canonical Allele Identifier: PA2826394614
Gene: PRRT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 940425
ClinVar RCV Id: RCV001210009

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243372.1:p.Ser90Arg
CA395477929
NM_001256443.2:c.268A>C
CA395477943
NM_001256443.2:c.270C>A
CA395477946
NM_001256443.2:c.270C>G