Canonical Allele Identifier: PA2825481071
Gene: SCN3A HGNC NCBI

Linked Data

ClinVar Variation Id: 432534
ClinVar RCV Id: RCV000498016 RCV001799670 RCV003446092 RCV003992303
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001075146.1:p.Arg1572Gln
CA349018276
NM_001081677.2:c.4715G>A