Canonical Allele Identifier: PA2825537401
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1405082
ClinVar RCV Id: RCV003541504 RCV004010833
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Ser20Phe
CA056785
NM_001099404.2:c.59C>T