Canonical Allele Identifier: PA2826394838
Gene: PRRT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2963631
ClinVar RCV Id: RCV003825269
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243372.1:p.Met280Ile
CA395480055
NM_001256443.2:c.840G>A
CA395480058
NM_001256443.2:c.840G>C
CA395480059
NM_001256443.2:c.840G>T