Canonical Allele Identifier: PA120369
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 9396
ClinVar RCV Id: RCV000009998 RCV000058832 RCV000148857 RCV000151804 RCV000258831 RCV000251727 RCV000586618 RCV000622951 RCV000678935 RCV001841241 RCV004528099
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Thr220Ile
CA019690
NM_000335.5:c.659C>T