Canonical Allele Identifier: PA645453430
Gene: SCN4A HGNC NCBI

Linked Data

ClinVar Variation Id: 324537
ClinVar RCV Id: RCV000263270 RCV000298352 RCV000299745 RCV000391174 RCV000416101 RCV000576587 RCV001086523 RCV004537819
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000325.4:p.His599Arg
CA8709746
NM_000334.4:c.1796A>G