Canonical Allele Identifier: PA2825127726
Gene: SCN4A HGNC NCBI

Linked Data

ClinVar Variation Id: 3068640
ClinVar RCV Id: RCV003994709
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000325.4:p.Lys1509Asn
CA400615826
NM_000334.4:c.4527G>T
CA400615827
NM_000334.4:c.4527G>C