Canonical Allele Identifier: PA2580109087
Gene: SCN4A HGNC NCBI

Linked Data

ClinVar Variation Id: 2435746
ClinVar RCV Id: RCV003136496 RCV003358144
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000325.4:p.Val1644Leu
CA8708873
NM_000334.4:c.4930G>C
CA292956761
NM_000334.4:c.4930G>T