Canonical Allele Identifier: PA2827921558
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 68049
ClinVar RCV Id: RCV000058852 RCV000154846 RCV000618432 RCV001842413 RCV004537263
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341630.1:p.Ala286Ser
CA019856
NM_001354701.2:c.856G>T