Canonical Allele Identifier: PA261121
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 39444
ClinVar RCV Id: RCV000032639 RCV000058833 RCV000211852 RCV000182941 RCV000678965 RCV000763109
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Arg222Gln
CA019704
NM_000335.5:c.665G>A