Canonical Allele Identifier: PA916056232
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 658093
ClinVar RCV Id: RCV003541009 RCV003591781 RCV002336688
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Ile1603Phe
CA352143580
NM_198056.3:c.4807A>T