Canonical Allele Identifier: PA107560
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67766
ClinVar RCV Id: RCV000058536 RCV001842320
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Arg971Cys
CA016616
NM_198056.3:c.2911C>T