Canonical Allele Identifier: PA2830430237
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 3070818
ClinVar RCV Id: RCV004013328
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Met801Leu
CA352143251
NM_198056.3:c.2401A>T
CA352143253
NM_198056.3:c.2401A>C