Canonical Allele Identifier: PA2573168031
Gene: SCN4A HGNC NCBI

Linked Data

ClinVar Variation Id: 1497142
ClinVar RCV Id: RCV001992245
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000325.4:p.Met576Leu
CA400633329
NM_000334.4:c.1726A>T
CA400633337
NM_000334.4:c.1726A>C