Canonical Allele Identifier: PA351983
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 222802
ClinVar RCV Id: RCV000208365
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Ala242Val
CA351979
NM_000335.5:c.725C>T