Canonical Allele Identifier: PA351018
Gene: SCN4A HGNC NCBI
ClinVar RCV:
RCV000207008
ClinVar Variation:
221261
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000325.4:p.Asn440Lys
CA351017
NM_000334.4:c.1320T>G
CA400635046
NM_000334.4:c.1320T>A