Canonical Allele Identifier: PA645506387
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 406444
ClinVar RCV Id: RCV000622063 RCV001841360 RCV002496752 RCV003766545
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Arg1897Gln
CA064637
NM_198056.3:c.5690G>A