Canonical Allele Identifier: PA2825844439
Gene: SCN4B HGNC NCBI

Linked Data

ClinVar Variation Id: 1331417
ClinVar RCV Id: RCV001806761
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135820.1:p.Asn26Lys
CA6300190
NM_001142348.2:c.78C>G
CA382777629
NM_001142348.2:c.78C>A