Canonical Allele Identifier: PA108701
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67651
ClinVar RCV Id: RCV000058408 RCV000157478 RCV000182964 RCV000234790 RCV000621361
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Val411Met
CA014560
NM_198056.3:c.1231G>A