Canonical Allele Identifier: PA145149
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 68014
ClinVar RCV Id: RCV000058810 RCV000183135 RCV000208349 RCV000249083 RCV001150126 RCV001150127 RCV001150128 RCV001192713 RCV001148566 RCV001148567 RCV001148565 RCV001842396 RCV003486638
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Val1950Met
CA019505
NM_000335.5:c.5848G>A