Canonical Allele Identifier: PA2825844436
Gene: SCN4B HGNC NCBI

Linked Data

ClinVar Variation Id: 1397893
ClinVar RCV Id: RCV001912656 RCV002334836
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135820.1:p.Glu23Gln
CA6300191
NM_001142348.2:c.67G>C