Canonical Allele Identifier: PA108608
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 9375
ClinVar RCV Id: RCV000009969 RCV000058778 RCV001561910 RCV002345237
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Tyr1795Cys
CA019196
NM_198056.3:c.5384A>G