Canonical Allele Identifier: PA329950
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67777
ClinVar RCV Id: RCV000058548 RCV001553202
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Arg104Gly
CA016820
NM_000335.5:c.310C>G