Canonical Allele Identifier: PA302215
Gene: SCN4B HGNC NCBI

Linked Data

ClinVar Variation Id: 190889
ClinVar RCV Id: RCV000619472 RCV001216410 RCV001698986
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_777594.1:p.Asp6Glu
CA302213
NM_174934.4:c.18C>A
CA382780525
NM_174934.4:c.18C>G