Canonical Allele Identifier: PA2825844425
Gene: SCN4B HGNC NCBI

Linked Data

ClinVar Variation Id: 190889
ClinVar RCV Id: RCV000619472 RCV001216410 RCV001698986
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135820.1:p.Asp6Glu
CA302213
NM_001142348.2:c.18C>A
CA382780525
NM_001142348.2:c.18C>G