Canonical Allele Identifier: PA2499298028
Gene: PRRT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1062259
ClinVar RCV Id: RCV001371955
ClinVar Variation Id: 2174878
ClinVar RCV Id: RCV002588220
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_660282.2:p.Met11Leu
CA7994465
NM_145239.3:c.31A>T
CA395477024
NM_145239.3:c.31A>C