Canonical Allele Identifier: PA2580109073
Gene: SCN4A HGNC NCBI

Linked Data

ClinVar Variation Id: 2055360
ClinVar RCV Id: RCV002947228

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000325.4:p.Asp1628Glu
CA8708886
NM_000334.4:c.4884C>A
CA400614612
NM_000334.4:c.4884C>G