Canonical Allele Identifier: PA235715
Gene: SCN4B HGNC NCBI

Linked Data

ClinVar Variation Id: 190891
ClinVar RCV Id: RCV000171074 RCV000619132 RCV001078793
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_777594.1:p.His65Leu
CA235713
NM_174934.4:c.194A>T