Canonical Allele Identifier: PA307734
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67942
ClinVar RCV Id: RCV000058727 RCV000183091 RCV001842373 RCV004019056
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Thr1644Met
CA018766
NM_000335.5:c.4931C>T