Canonical Allele Identifier: PA645396373
Gene: SCN4B HGNC NCBI

Linked Data

ClinVar Variation Id: 302646
ClinVar RCV Id: RCV002494949 RCV001549670 RCV003380546 RCV000353970
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_777594.1:p.Thr161Arg
CA6300188
NM_174934.4:c.482C>G