Canonical Allele Identifier: PA2825128127
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 2758252
ClinVar RCV Id: RCV003569598
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Met28Thr
CA056895
NM_000335.5:c.83T>C