Canonical Allele Identifier: PA120356
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 9393
ClinVar RCV Id: RCV000009992 RCV000009993 RCV000058563 RCV000041615 RCV000204216 RCV000274325 RCV000304064 RCV000363449 RCV000368908 RCV000396768 RCV000621429 RCV000755696 RCV001094834 RCV001841239 RCV003125829 RCV003149567 RCV002504776
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Ser1103Tyr
CA017028
NM_198056.3:c.3308C>A