Canonical Allele Identifier: PA2580159893
Gene: SCN4B HGNC NCBI

Linked Data

ClinVar Variation Id: 2447643
ClinVar RCV Id: RCV003176551
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135821.1:p.Val42Ala
CA6300213
NM_001142349.2:c.125T>C