Canonical Allele Identifier: PA329868
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67711
ClinVar RCV Id: RCV000058478 RCV001811346 RCV003162455 RCV003224132 RCV001842309
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Ala691Thr
CA015822
NM_001099404.2:c.2071G>A