Canonical Allele Identifier: PA093064
Gene: SCN4A HGNC NCBI

Linked Data

ClinVar Variation Id: 143200
ClinVar RCV Id: RCV000132736 RCV000395392 RCV000547264 RCV000995863 RCV001127055 RCV001127056
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000325.4:p.Arg1129Gln
CA345719
NM_000334.4:c.3386G>A