Canonical Allele Identifier: PA265920
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 68039
ClinVar RCV Id: RCV000058842 RCV000182946 RCV001842411 RCV003162462
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Val240Met
CA019765
NM_001099404.2:c.718G>A