Canonical Allele Identifier: PA2825944735
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 924677
ClinVar RCV Id: RCV001843279 RCV003660867
ClinVar Variation Id: 1023804
ClinVar RCV Id: RCV001729846 RCV004005120
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153633.1:p.Met1191Ile
CA062231
NM_001160161.2:c.3573G>A
CA352149230
NM_001160161.2:c.3573G>T
CA352149231
NM_001160161.2:c.3573G>C