Canonical Allele Identifier: PA218892
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67770
ClinVar RCV Id: RCV000058540 RCV000417955 RCV001147137 RCV001147139 RCV001147138 RCV001147140 RCV001147141 RCV001147142 RCV001842323 RCV004019045
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Arg986Gln
CA016672
NM_198056.3:c.2957G>A