Canonical Allele Identifier: PA2825130854
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 926342
ClinVar RCV Id: RCV001841060
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Gly1157Val
CA352138401
NM_000335.5:c.3470G>T