Canonical Allele Identifier: PA2573062294
Gene: SCN4A HGNC NCBI

Linked Data

ClinVar Variation Id: 1306041
ClinVar RCV Id: RCV001766994
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000325.4:p.Asn1570His
CA400615319
NM_000334.4:c.4708A>C