Canonical Allele Identifier: PA915978554
Gene: SCN4B HGNC NCBI

Linked Data

ClinVar Variation Id: 302646
ClinVar RCV Id: RCV002494949 RCV001549670 RCV003380546 RCV000353970
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135821.1:p.Thr51Arg
CA6300188
NM_001142349.2:c.152C>G