Canonical Allele Identifier: PA2825538832
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 406416
ClinVar RCV Id: RCV001841352 RCV003766538
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Met1214Thr
CA16611463
NM_001099404.2:c.3641T>C