Canonical Allele Identifier: PA2573062293
Gene: SCN4A HGNC NCBI

Linked Data

ClinVar Variation Id: 1300174

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000325.4:p.Pro1560Leu
CA8708918
NM_000334.4:c.4679C>T