Canonical Allele Identifier: PA2825132598
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 3071902
ClinVar RCV Id: RCV004011932
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Met1867Thr
CA352140673
NM_000335.5:c.5600T>C