Canonical Allele Identifier: PA108688
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_932173.1:p.Val1951Met
CA019505
NM_198056.3:c.5851G>A