Canonical Allele Identifier: PA2827922776
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67788
ClinVar RCV Id: RCV000058561 RCV001147832 RCV001089363 RCV001147831 RCV001147833 RCV001147830 RCV001149365 RCV001149366 RCV002321560 RCV001842331 RCV003235025
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341630.1:p.Val1097Leu
CA017002
NM_001354701.2:c.3289G>T
CA352138792
NM_001354701.2:c.3289G>C