Canonical Allele Identifier: PA329844
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67696
ClinVar RCV Id: RCV000058460 RCV003541028
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Pro637Leu
CA015533
NM_000335.5:c.1910C>T