Canonical Allele Identifier: PA1139759521
Gene: PRRT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 940425
ClinVar RCV Id: RCV001210009

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_660282.2:p.Ser90Arg
CA395477929
NM_145239.3:c.268A>C
CA395477943
NM_145239.3:c.270C>A
CA395477946
NM_145239.3:c.270C>G