Canonical Allele Identifier: PA2741815527
Gene: SCN4A HGNC NCBI

Linked Data

ClinVar Variation Id: 2768804
ClinVar RCV Id: RCV003505621

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000325.4:p.Leu1587del
CA2697555062
NM_000334.4:c.4759_4761del