Canonical Allele Identifier: PA2580159894
Gene: SCN4B HGNC NCBI

Linked Data

ClinVar Variation Id: 1741691
ClinVar RCV Id: RCV002342258
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135821.1:p.Asp43Gly
CA6300211
NM_001142349.2:c.128A>G